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Hypermobility symptoms

Hypermobile Ehlers-Danlos syndrome Genetic and Rare

Joint hypermobility symptoms and treatments - Illnesses

Top 10 Most Common Symptoms of Hypermobility Syndrome

Symptoms Children or young adults with hypermobility have joint pain. The pain is more common in the legs, such as the calf or thigh muscles. It most often involves large joints such as the knees.. Joint hypermobility can be symptomless apart from the unusual mobility, but there is a series of other symptoms that result from that mobility. These should be evaluated for a diagnosis of HSD (and treated, of course). Trauma. Macrotrauma includes dislocation, subluxations, and connective soft tissue damage (ligaments, tendons, muscles) It's important not to over-medicalise hypermobility or create unnecessary fear as around 10% of the population is hypermobile - but most have no symptoms. HSD can only be diagnosed when other conditions have been excluded, eg EDS, Marfans or Downs syndrome, where joint laxity is part of the condition Symptoms of joint hypermobility syndrome include: Muscle strain or pain (especially after hard physical work or exercise) - Your muscles have to work harder if your joints are very supple and this can lead to muscle strain and a general feeling of fatigue

The most common symptoms of joint hypermobility syndrome include: Joint pain (often worsened late in the day This is called benign hypermobility syndrome since the only symptom is hypermobile joints. It can be caused by: bone shape or the depth of the joint sockets. muscle tone or strength. a poor sense. Hypermobility Syndrome Symptoms For people with hypermobility syndrome, it can be hard to gauge the excessive movement of the joints in some situations. As non-benign cases usually present other signs and symptoms, it is crucial to recognize what can and cannot be treated Urethral hypermobility is defined as incompetence of the urethral sphincter mechanisms usually associated with stress incontinence symptoms, due to failure of urethral support. Stress incontinence is the involuntary loss of urine with increased intraabdominal pressure or physical exertion (coughing, sneezing, jumping, lifting, exercise)

Ehlers-Danlos Syndrome ( hypermobility type) is characterized by signs and symptoms similar to joint hypermobility. Muscular, integumentary, and skeletal problems are common. EDS involves hypermobility in joints of elbows, knees, toes, fingers, skin problems, easy bruising of the skin, long-term pain in muscles and bones that are non-responsive. Joint hypermobility syndrome is when you have very flexible joints and it causes you pain (you may think of yourself as being double-jointed). It usually affects children and young people and often gets better as you get older. See a GP if you: often get tired, even after res

Zarate N, Farmer AD, Grahame R, et al. Unexplained gastrointestinal symptoms and joint hypermobility: is connective tissue the missing link? Neurogastroenterol Motil 2010; 22:252. Fikree A, Grahame R, Aktar R, et al. A prospective evaluation of undiagnosed joint hypermobility syndrome in patients with gastrointestinal symptoms TMJ Hypermobility: How to assess. So what exactly is TMJ hypermobility? Well hypermobility is characterized by early and/or excessive forward gliding (translating) of one or both TMJs. This excessive forward gliding results in laxity of the surrounding capsule and ligaments and the temporalis tendon. The over-stretching of these structures over.

Joint hypermobility — the ability of a joint to move beyond its normal range of motion — is common in children and decreases with age. Having a few hypermobile joints isn't unusual. In most people, joint hypermobility causes no problems and requires no treatment. But in some people, hypermobility causes joint pain and may result in a higher. A Hypermobility Disorder (HD) is an umbrella term that generally describes someone who has hyper mobile joints with symptoms. A hyper mobile joint is not a disease or a diagnosis. It simply describes a joint that moves a greater than average range of motion. It becomes a disorder when it starts to cause symptoms such as pain, instability. Hypermobility spectrum disorder (HSD), related to earlier diagnoses such as hypermobility syndrome (HMS), and joint hypermobility syndrome (JHS) is a heritable connective tissue disorder that affects joints and ligaments. Different forms and sub-types have been distinguished, but it does not include asymptomatic joint hypermobility, sometimes known as double-jointedness Joint hypermobility without pain occurs when children have stretchy or flexible joints, but without exercise-related pain. This is an advantage to some children, and tends to be associated with being good at sport. HSDs are the diagnosis where the main or only symptoms are exercise-related pain, together with joint hypermobility

Hypermobility syndrome is estimated to affect between 10%-25% of the population, although severity may vary. A disorder that causes the joints to extend beyond the normal range, hypermobility is one variation of a more generalized diagnosis known as Ehlers-Danlos Syndrome There are many associated symptoms and disorders which don't form part of the formal criteria, and which do not directly result from joint hypermobility, for instance orthostatic tachycardia, digestive disorders, pelvic and bladder dysfunction, and anxiety disorders. These are often more detrimental to quality of life than the joint symptoms

Hypermobility can be called a problem that is related to muscles and bones, although it has nothing to do with body movement. If you have this problem, from time to time, you will have pain or various symptoms of hypermobility Symptoms Associated with Hypermobility Syndromes When Hypermobility syndromes are present, the same excessive connective tissue flexibility that is present in the joints can be associated with many other symptoms, which must be diagnosed and treated individually. Below, is a partial list of symptoms and signs that patients with joint. There is substantial symptom overlap between the EDS subtypes and the other connective tissue disorders including hypermobility spectrum disorders, as well as a lot of variability, so a definitive diagnosis for all the EDS subtypes when the gene mutation is known—all but hypermobile EDS (hEDS)—also calls for confirmation by testing to.

What are hypermobility syndromes? Hypermobility

Symptoms of the hypermobility of the spine. The clinical picture is different in that a person develops increased mobility and flexibility in the joints. It is characterized by increased mobility of the joints located between the vertebrae. The main symptom is back pain. The main reason is considered to be genetic disorders in the development. TMJ Hypermobility: How to assess. So what exactly is TMJ hypermobility? Well hypermobility is characterized by early and/or excessive forward gliding (translating) of one or both TMJs. This excessive forward gliding results in laxity of the surrounding capsule and ligaments and the temporalis tendon. The over-stretching of these structures over. Be Aware of Hypermobility's Symptoms People with hypermobile joints can usually move their joints beyond the normal range. Yet, a professional should document this unusual flexibility and compare it to established norms. Being bendy can have consequences like muscle pain, bruising, fatigue and injury Symptoms range across a wide spectrum and include joint hypermobility, stretchy and velvety skin, chronic pain in the bones and muscles, osteoporosis, osteoarthritis, gastrointestinal (GI) tract issues, heart and blood vessel issues, and female-related health issues such as painful menstruation and pregnancy complications These symptoms are often due to a sudden change in posture, but sometimes occur after eating as well. A recent study showed that autonomic symptoms and gastrointestinal symptoms are the two areas most likely to have an impact on the quality of life for EDS sufferers (hypermobile, classical and vascular types)

joints and soft, velvety skin, as well as other symptoms almost identical to those described here. For most people, the distinction between joint hypermobility, joint hypermobility syndrome, and the hypermobile type of Ehlers-Danlos is not an important one clinically, as treatments are similar. Exceptions include mor The Spectrum of Hypermobility. Hypermobility is excess (hyper) movement (mobility) present in the joints of the human body. This is the opposite of hypomobility, the decrease of movement in the joint. Many disorders and diseases diagnosed and managed by Rheumatologists involve hypomobility - the most common being Arthritis The more difficult question to answer is if you do have hypermobility and related issues, do you have a connective tissue disorder or a syndrome. The following information is designed to give those with hypermobility and associated symptoms some guidance on where to go and what to do to manage their symptoms Symptoms of hypermobility spectrum disorders may resolve with therapy, persist, or progress to hypermobile EDS. Hypermobile EDS is managed as a lifelong condition because no curative treatments.

The new Hypermobility Spectrum Disorders. As you can see, both the top three, (in purple) asymptomatic and next three (in black text) symptomatic forms come in 3 flavors: Generalized Joint Hypermobility (you pass with a high Beighton hypermobility Score) Peripheral Joint Hypermobility (it's typically limited to hands and/or feet Ds1 does also have low muscle tone. According to ds1's physio, the real harm of the w-position is caused where a child's hypermobility/low tone is neurological (ie the brain reacts too slowly to damaging over-stretching of muscles and ligaments that would not otherwise be naturally that stretchy) Minor symptoms may include bruising that doesn't always seem to have a cause, bruising in unusual areas like your cheeks or back, thin skin that looks almost translucent, a collapsed lung, skin that looks older than your age, clubfoot, hip dislocations, hypermobility or flexibility in your smaller joints, tendon or muscle ruptures, thinning.

Hypermobility syndrome can also be associated with postural orthostatic tachycardia syndrome (POTS). Symptoms. Hypermobility tends to run in families, and girls are usually more symptomatic than boys. Not all children with hypermobility experience pain or inflammation, and it is unknown why some children develop pain while others do not Joint hypermobility disorders are associated with three recognized inheritable disorders of connective tissue. There are three principle disorders that must be considered when a patient shows signs and symptoms of hypermobility to include 1) Marfan syndrome (MFS), 2) Ehlers-Danlos syndrome (EDS) and 3) Benign joint hypermobility syndrome (BJHS) The symptoms of the Hypermobility Syndrome are very important to notice. Sometimes, the symptoms are ignored because of the general tendency that could add sufferings for the patient. So, it is advisable to understand the symptoms of the Hypermobility Syndrome. As this is a very common syndrome so you might come across such situation and then. Symptoms associated with EDS Type III are joint pain, hypermobility, mild extra-articular involvement, and mild skin changes without scarring. It has therefore been proposed that BJHS may indeed be a mild form of EDS - and that the two conditions are really a continuum • Hypermobility Spectrum Disorder (HSD) is the most common systemic inherited connective tissue disorder in humans - In the UK prevalence of HSD associated with chronic widespread pain or severely disabling pain (Mulvey, et al, 2013) is almost as high as fibromyalgia (Fayaz et al, 2016) and 100 times higher than rheumatoi

Symptoms of Ehlers-Danlos syndromes (EDS) There are several types of EDS that may share some symptoms. These include: an increased range of joint movement (joint hypermobility) stretchy skin. fragile skin that breaks or bruises easily. EDS can affect people in different ways. For some, the condition is relatively mild, while for others their. Hypermobility can make it difficult to get restful sleep and chronic pain can also cause sleep disturbances which will leave you feeling even more tired. As well as hypermobility and fatigue, there are a small number of other symptoms including issues with the digestive system and a tendency to suffer from strains and sprains and chronic pain Hypermobility Spectrum Disorder (HSD) is a protein disorder recently specified in the reclassification of the Ehler's-Danlos family of connective tissue disorders with many neurological symptoms. Because of the overlap of symptoms and MRI in HSD and MS, it should be considered an MS Mimic, and looked for when the diagnosis of MS is. hEDS is mainly identified by generalized joint hypermobility (GJH), additional joint issues, and obvious skin signs, which are less severe than those seen in Classic EDS (cEDS) or Vascular EDS (vEDS). hEDS is more than just GJH plus a few items from a checklist of findings

Ehlers-Danlos syndromes are a group of connective tissue disorders that can be inherited and are varied both in how affect the body and in their genetic causes. They are generally characterized by joint hypermobility (joints that stretch further than normal), skin hyperextensibility (skin that can be stretched further than normal), and tissue fragility Hypermobile joints, also known as loose joints, describes the ability of a joint to move beyond its normal range of motion. People with hypermobile joints are sometimes referred to as being double jointed. Benign hypermobility syndrome can lead to weak, loose ligaments and joint instability Her Cervical spine is so hypermobile that the muscles surrounding the joints are always tense and sometimes will spasms. When the muscles spasms c5 will sublux and causes torticolis where her head turns to the side. C2 will then also sublux causing dizziness, headaches and severe pain. This started happening when she was 13 years old I've been hypermobile forever but it only became symptomatic as I hit early adulthood (like 17). Since then I have had fluctuating symptoms including but not limited to joint pain, joint instability, IBS, anxiety-like physical symptoms but no anxiety. I weight train and use cbd balm on my knees and shoulders. But holy hell this week has knocked me The hypermobility syndrome(HMS) was first described in 1967 by Kirk et al as the occurrence of musculoskeletal symptoms in hypermobile healthy persons.[1] Meanwhile, other names are given to HMS, such as joint hypermobility syndrome and benign hypermobility joint syndrome. HMS is a dominant inherited connective tissue disorder described as generalized articular hypermobility, with or.

HYPERMOBILITY TYPE EDS The clinical diagnosis of hEDS requires the simultaneous presence of criteria 1 AND 2 AND 3. Criterion 1: Generalized joint hypermobility (GJH) • The Beighton score: ≥6 for pre-pubertal children and adolescents, ≥5 for pubertal men and women up to the age of 50, and ≥4 for those >50 years of age for hEDS Joint hypermobility is common among in young females and is seen in about 5% of the healthy adult population. When musculoskeletal symptoms occur in hypermobile people in the absence of any other systemic rheumatological disorder, it is called hypermobility syndrome

Generalized joint hypermobility (GJH) and joint hypermobility syndrome (JHS) are gaining increased attention as potential sources of pain and injury. The aims of this study were to evaluate prevalence of GJH and JHS and to determine whether musculoskeletal injuries and symptoms commonly attributed t The joint hypermobility syndrome is a condition in which the joints easily move beyond the normal range expected for a particular joint. The condition tends to run in families. Symptoms of hypermobility syndrome include joint pain. People with hypermobility syndrome are more susceptible to injury, including dislocations and sprains Orthopaedic surgery in hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders. A look at the pros and cons of opting for orthopaedic surgery if you have hypermobile Ehlers-Danlos syndrome or a hypermobility spectrum disorder, and a discussion of the special measures that need to be taken. Footcare in hypermobile Ehlers-Danlos. This pattern of symptoms is sometimes called Joint hypermobility syndrome (JHS) and can include a diagnosis of Hypermobile type Ehlers-Danlos Syndrome (h-EDS). Joint hypermobility is treated with a rehabilitation program of physical strengthening and reconditioning in conjunction with pain management psychological strategies to help. Hypermobility describes joints that stretch farther than is normal. Hypermobility syndrome is used to describe a disorder in which musculoskeletal pain and generalized joint hypermobility occur together. Common symptoms reported by people with hypermobility syndrom

Joint hypermobility syndrome can cause a wide range of symptoms, including symptoms that affect your digestive system and blood pressure (read more about the symptoms of joint hypermobility). It will be necessary to assess the effect of all your symptoms on your quality of life and ability to carry out every day tasks Hypermobility syndrome or HMS may also occur in the genetic and chromosomal disorders like in Down syndrome and also in the metabolic disorders. There are various symptoms of Hypermobility syndrome, of which the primary being excessive laxity of multiple joints Joint hypermobility disorders are associated with three recognized inheritable disorders of connective tissue. There are three principle disorders that must be considered when a patient shows signs and symptoms of hypermobility to include 1) Marfan syndrome (MFS), Figure 1. The Acrobat Ceramic Art from Tlatilco Dated 1200 - 900 BC Hypermobility Syndromes and Hypermobility Spectrum Disorder What are Hypermobility Syndromes: Benign Hypermobility Syndrome affects perhaps 5% of the population, and is diagnosed when joint hypermobility is present on a simple joint flexibility score called the Beighton Score, which is equal to or greater than 5

There are other symptoms which may also be part of hypermobility disorders, such as fatigue, light-headedness, and digestive issues, to name a few. (Again, this is why it's so important to check in with a medical professional!) Patients with joint hypermobility syndrome of knee are referred to as having double jointed knee which is an inherited condition that occurs when certain genes are passed on to the children by their parents. Know the causes, symptoms, treatment, risk factors and prognosis of joint hypermobility syndrome of knee or double jointed knee Infant hypermobility is a common asymptomatic condition in children under the age of 5 that causes joints to move outside their normal limits. It occurs when collagen levels in tendons and ligaments are altered, making the fibers thinner and less stiff. It occurs, on average, in 30% of the child population, being more common in girls than in boys, in a ratio of 3 to 1 Joint hypermobility syndrome (JHS), previously known as benign joint hypermobility syndrome (BJHS), is a heritable disorder of connective tissue that comprises symptomatic hypermobility predisposing to arthralgia, soft tissue injury, and joint instability.1 It is indistinguishable from the hypermobility type of Ehlers-Danlos syndrome.2 Complications may include autonomic dysfunction.

Hypermobility Syndrome Symptoms, Signs & Caus

  1. For many people, hypermobile joints are painless and not caused by an underlying medical issue, but for some, hypermobility can be a painful symptom of a chronic condition - such as Ehlers-Danlos syndrome, joint hypermobility syndrome or Marfan syndrome. Although it can sometimes take years (perhaps even decades) to receive a diagnosis that.
  2. Joint hypermobility syndrome (JHS) is a connective tissue disorder that primarily affects the musculoskeletal system. All of these disorders may present with symptoms referable to joint hypermobility, including joint pain, swelling, instability, and dislocation, as well as back pain. Concern regarding the presence of the more severe MFS or EDS.
  3. EDS is defined as a more-than-normal range of movement (ROM) in a joint, is either localized (increased range of motion in a single joint) or generalized throughout the body. There are 13 types of EDS, with a variety of symptoms and severity. Joint hypermobility may vary based on age, gender, family and ethnic background

The Symptoms I Had That Were Signs of Hypermobility The

  1. When hypermobility is accompanied by symptoms like these, we call it JHS (Joint Hypermobility Syndrome). What causes hypermobility? In many cases, hypermobility occurs independently of any other conditions. In other words, hypermobility isn't always the result of an underlying health issue - some people are just double-jointed with no clear cause
  2. exhibit symptoms of generalized joint hypermobility (GJH; Criterion 1) exhibit systemic manifestations of a more generalized connective tissue disorder or have a positive family history or exhibit musculoskeletal complications (all Criterion 2) and be evaluated to exclude other EDS or connective tissue disorder diagnoses (Criterion 3).
  3. Adolescence is a time of huge change. All of us who have been through it remember all the changes, and the challenges they bring. Add to that tumultuous time a diagnosis, or undiagnosed symptoms of hypermobility or any other major medical condition and that time can be a nightmare

Hypermobility is a body type and as such there is no cure. The treatment therefore focuses on minimising the symptoms. Children might be referred to a physiotherapist and/or an occupational therapist to help improve their balance, coordination, muscle strength and fitness so their joints are better protected Hypermobility Disorder Care and Research for Children and Young Adults. The Hypermobility Clinic provides care and treatment to patients ages 6-22 with hypermobility disorders, including hypermobility spectrum disorder and hypermobile Ehlers-Danlos syndrome (hEDS). Our team includes a pediatrician, an advanced practice registered nurse, genetic. Welcome to Hypermobility Connect, an online community & education source for people with hypermobility conditions including The Hypermobility Spectrum Disorders, The Ehlers-Danlos Syndromes, Loeys-Dietz, Marfan & Stickler Syndromes and Osteogenesis Imperfecta. Based in Australia, supporting people across the globe Hypermobility-type EDS is often characterized by joint hypermobility, joint instability, and joint pain. While some connective tissue disorders are associated with specific and distinctive features, there may be symptoms that overlap between EDS types or other connective tissue disorders

Hypermobility may be present alone without any other symptoms. However many limitations are observed such as muscle fatigue and a general predisposition to joint dislocation Knoxville Tennessee Orthopedic Surgeon Doctors physician directory - The joint hypermobility syndrome is a condition in which the joints easily move beyond the normal range expected for a particular joint. The condition tends to run in families. Symptoms of hypermobility syndrome include joint pain. People with hypermobility syndrome are more susceptible to injury, including dislocations and.

Hypermobility Syndrome Tests, Symptoms, and Treatmen

Back in October I hurt my hip on a run with my drill sergeant. After months of fighting to be diagnosed last week I was. I finally had confirmation from a doctor saying that I have EDS hypermobility and that all the doctors before that told me I had zero chance at staying in the service were right New York New York Orthopedic Surgeon Doctors physician directory - The joint hypermobility syndrome is a condition in which the joints easily move beyond the normal range expected for a particular joint. The condition tends to run in families. Symptoms of hypermobility syndrome include joint pain. People with hypermobility syndrome are more susceptible to injury, including dislocations and. The so-called Benign Hypermobility Syndrome may not be so benign after all. Benign Hypermobility Syndrome is frequently associated with joint pain, fatigue due to mild sleep disordered breathing, blood pressure regulation (POTS), gastrointestinal issues like Irritable Bowel syndrome, headache, Hashimoto's thyroiditis, and. Some doctors believe that hEDS is a more severe form of hypermobility syndrome and there is certainly an overlap in symptoms. However, hypermobility syndrome mainly affects joints. EDS is more likely to be the diagnosis where there are associated, more serious conditions, such as heart valve problems, prolapse or repeated dislocations Introduction Many patients who come to our Headache Center have joint hypermobility in addition to their headaches, and they often also have sleep problems, joint problems, and symptoms of dysautonomias such as red hands and feet, fatigue, and GI problems. Because of the high prevalence of these symptoms in our headache patients, we decided to investigate further the relationship between these.

The Unexpected Symptoms of Hypermobility The Might

An unusually large range of joint movement (hypermobility) occurs in most forms of Ehlers-Danlos syndrome, and it is a hallmark feature of the hypermobile type. Infants and children with hypermobility often have weak muscle tone (hypotonia), which can delay the development of motor skills such as sitting, standing, and walking Infants with joint hypermobility have joints that are able to bend further than usual and a trunk and limbs that appear to be floppy and weak. The increased range of movement at the joints (sometimes called joint laxity or being double jointed) is due to differences in the connective tissue that forms the joint capsule and ligaments I've had symptoms of joint hypermobility syndrome since a teenager. I am now 65 and up to 10 years ago I was misdiagnosed over and over. It has gotten worse over time with symptoms of sublimation in hips and knees. Major and minor joints are extremely painful and I take opioid medication to help The isometric contraction of the muscles surrounding joints with hypermobility may help strengthen the ability to maintain neutral joint positions while holding instruments. Athletic tape and small finger splints for joint stability can be used as temporary props if pain or discomfort develops (Figure 5, page 26). 1,17

Are You Hyperflexible? The Neurology of Hypermobility

Symptoms of Hypermobility Syndrome. The symptoms of Joint Hypermobility Syndrome can affect different parts of the body; if the pain is one of the symptoms, it will usually be in the fingers, knees, hips, elbows, wrist, and shoulders. The symptoms of JHS include: Pain and Stiffness in the Joints and muscles (especially near the end of the day Joint hypermobility predisposes individuals in some sports to injury more than other sports. Gebska et al. (2016) found that swimmers with joint hypermobility were more likely to sustain injuries to the shoulder and elbow than were rowers. Specifically, almost 80% of the injuries in swimmers with hypermobility were classified as overuse. Following on from our Top 5 Kitchen Aids from our #HypermobilityHelp series, it's time to look at the general aids for hypermobility that I have found helpful for living with hypermobility.. Please note all links in this post except those marked Official Website or otherwise stated, are affiliate links. Affiliate links are going to help us keep Hypermobility Connect online

Joint hypermobility - MEpediaRheumatology for patients » Hypermobility syndrome

Benign Hypermobility Joint Syndrome: Symptoms, Causes

We performed a single-center retrospective study on the incidence of head and neck symptoms in 140 patients with hypermobility disorders over a 2-year period. Overall, 93 patients (66%) reported either headache or neck pain with 49 of those (53%) reporting both. Migraine (83%) was the most common headache type among those with headache. Expected Outcomes• Having a general understanding of what Ehlers-Danlos Syndrome is and what the symptoms are.• Distinguishing between the 3 most prominent types of EDS.• Understanding the heritability of EDS as a genetic disorder.• Learning how to score a patient on the Beighton criteria to determine the degree of hypermobility. 3

Ehlers-Danlos Syndrome & Hypermobility22 ‘Habits’ of People With Ehlers-Danlos Syndrome | The MightyHYPERMOBILE HIP DYSPLASIA CAM FAIS deformity gives chronicJoint hypermobility in infants -- to to assess | EDS

Hypermobility syndrome is the term used to describe otherwise healthy individuals who exhibit generalized hypermobility associated with musculoskeletal complaints. The term was coined in 1967 by Kirk and colleagues, who reported the occurrence of rheumatic symptoms in a group of hypermobile children 1998 Brighton criteria for classification of joint hypermobility syndrome • Joint hypermobility syndrome is diagnosed in the presence of two major criteria; one major criterion plus two minor criteria; or four minor criteria. Two minor criteria will suffice where there is an unequivocally affected first degree relative Although general joint hypermobility was not associated with ankle and foot outcomes, knee hypermobility was associated with ankle symptoms, foot symptoms, and talonavicular OA (adjusted odds ratios of 4.4, 2.4, and 3.0, respectively). CONCLUSION: Knee joint hypermobility may be related to talonavicular OA and to ankle and foot symptoms The most common type of EDS is known as Hypermobile EDS (hEDS) and although prevalence estimates aren't available due to the recency of changes within its diagnostic criteria, it is believed by most clinicians, researchers, and patients to be a common condition, occurring in greater than 1 in 2,000 people The original concept of the joint hypermobility syndrome (JHS) as a largely trivial complaint, whereby loose hypermobile joints give rise to aches, pains, strains, dislocations, and occasionally. dromes with joint hypermobility in that their symptoms are FIGURE 1 Atrophic scar. TABLE 1 (continued) Overlap between Joint Hypermobility, Hypermobility Spectrum Disorders, and Ehlers-Danlo