Benign joint hypermobility syndrome (BJHS) is a hereditable disorder of connective tissue, which is characterized by the occurrence of multiple musculoskeletal problems in hypermobile individuals who do not have a systemic rheumatological disease. Rectal, uterine and mitral prolapses, varicose veins, myopia and recurrent urinary tract infections are more common in patients with BJHS, which indicates a diffuse anomaly in the structure of connective tissue rather than a limited involvement of the musculoskeletal system. Asthma, as a complex trait disease, develops after environmental exposure to innocuous allergens, infectious agents and air pollutants in susceptible individuals on the basis of their genetics. However, genetic factors cannot explain the recent rise in the prevalence, morbidity, or mortality of asthma. Asthma may also be caused by a connective tissue defect. Changes in the mechanical properties of the bronchial airways and lung parenchyma may underlie the increased tendency of the ...

Abdominal and pelvic pain can have a variety of causes. Joint hypermobility syndrome can often be an undetected and underdiagnosed comorbidity in chronic pelvic pain conditions (I.e. like endometriosis). Joint hypermobility syndrome, or benign hypermobility syndrome, is a connective tissue disorder and considered a milder variant of Ehlers-Danlos Syndrome. This syndrome is characterized by chronic musculoskeletal pain as a consequence of joint hyperextensibility. Patients with this syndrome are commonly afflicted by pain in their pelvis, fingers, hips, knees, and elbows. A physician and/or physical therapist evaluates using special tests such as the Nine Point Beighton Score as a diagnostic tool to determine whether hypermobility is present.. Patients with joint hypermobility syndrome may display signs of fatigue, headaches, anxiety, orthostatic hypotension, and many experience abdominal and genitourinary difficulties at high rates. According to a 2013 study, about 3% of people have some form of ...

The extent and risk of knee injuries in children aged 9-14 with Generalised Joint Hypermobility and knee joint hypermobility - the CHAMPS-study Denmark ...

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Any score above 4 meets the Major criteria for hypermobility. Minor criteria includes any score 1-3, or greater than or equal to zero if aged 50+; and any of the criteria below. (from The Hypermobility Syndrome Association). · Arthralgia (, 3 months) in one to three joints or back pain (, 3 months), spondylosis, spondylolysis/spondylolisthesis.. · Dislocation/subluxation in more than one joint, or in one joint on more than one occasion.. · Soft tissue rheumatism. , 3 lesions (e.g. epicondylitis, tenosynovitis, bursitis).. · Marfanoid habitus (tall, slim, span/height ratio ,1.03, upper: lower segment ratio less than 0.89, arachnodactyly [positive Steinberg/wrist signs].. · Abnormal skin: striae, hyperextensibility, thin skin, papyraceous scarring.. · Eye signs: drooping eyelids or myopia or antimongoloid slant.. · Varicose veins or hernia or uterine/rectal prolapse Clinical hypermobility is indicative of more serious problems outside the musculoskeletal realm and may require separate ...

Beyond this, I may need to work on an appointment with a local EDS doctor. There are not many. Theres mostly only Dr. Brad Tinkle. I have heard there is a 2 year wait to see him. But sometimes, with a doctors referral, you can get in sooner. My only hesitation is based on fear. Im afraid, based on some stories Ive heard, that he may not acknowledge my EDS, now that my Beighton score is lower. Im only in my early 30s, but my joints have stiffened up as theyve become more painful with age. And the test for EDS mainly tests elbows, knees, and small joints of the fingers. My elbows and knees barely hyperextend anymore. A fellow blogger has recently posted about the problem with the Beighton and Brighton scores for EDS diagnosis: https://mastcellblog.wordpress.com/2016/02/16/bbscores/. I couldnt agree more. Im so glad I was diagnosed by Dr. Francomano in my 20s, when I was more flexible, with a Beighton score of 8/9. Anyway, this is my hesitation to see Dr. Tinkle. I dont want him to ...

Results: A total of 66 responses (80% women) were received from physiotherapists with a wide range of clinical experience. 68% of respondents reported that they had not received any formal training in JHS management. 69% of respondents reported not using the recommended Brighton diagnostic criteria for JHS. The stated aims of physiotherapy and the specific interventions employed seemed well matched, with a focus on advice, education, exercise and self-management. Although pain relief was not reported as a high priority in terms of treatment aims, pain was most often assessed as an outcome, suggesting a mismatch between what clinicians aim to achieve and what they measure ...

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EDS-HT, considered to be one and the same with joint hypermobility syndrome (JHS), is a relatively common, frequently underdiagnosed heritable condition which predisposes those afflicted to chronic, widespread musculoskeletal pain and a wide variety of articular and extra-articular features purportedly linked to constitutionally abnormal collagen. The diagnosis is primarily clinical in essence and is largely based on the Beighton score (a simple system used to quantify joint laxity and hypermobility) and medical history. It is predominantly of autosomal dominant inheritance, though the molecular basis of EDS-HT is still largely unknown except for a minority of patients mutated in TNXB and COL3A1 [4]. Skin biopsies may show alterations in collagen fibril morphology [5]. Early literature fixed the frequency of EDS as a whole to 1 in 5000, with EDS-HT accounting for approximately half of all registered cases. However, due to its vast underdiagnosis, a presumed frequency of 0.75-2% has been ...

The management of individuals with BJHS can be very challenging and there are no evidence-based management strategies currently available. Acute pain episodes are commonly managed using taping, bracing or splinting or with non-steroidal anti-inflammatory drugs as needed. However reassurance and a multi-disciplinary training program are the mainstays of long term management. Physical therapy is of the outmost importance, and encouraging an active lifestyle may improve function and enhance quality of life [20]. As general principles, strengthening exercises focused on muscles around hypermobile joints may help to enhance joint support throughout movement and reduce pain; closed chain exercises may enhance proprioceptive feedback and optimize muscle action. Proprioception may be improved also by coordination and balance exercises. Physical therapy should also encompass a generalized exercise programme, addressing cardio-respiratory, musculoskeletal and neurological aspects of movement with the aim ...

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Hypermobility syndrome refers to joints that move beyond the normal range with little effort. Joints most commonly affected are the fingers, wrists, elbows and knees.

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PhD Project - A study of the natural history of joint hypermobility using a population-based birth cohort at University of Bristol, listed on FindAPhD.com

Comprehensively relates practical therapy to the nature of the underlying pathology Covers in one single text both the scientific and practical management aspect of Joint Hypermobility Syndrome and its allied pathologies Contributions from over 30 leadin

Protiere, S. ; Bazant, M. Z. ; Weitz, D. A. ; Stone, H. A. Droplet breakup in flow past an obstacle: A capillary instability due to permeability variations. Epl 2010, 92.

in Journal of Novel Physiotherapies (2013), 3(6), 1805. Introduction: Joint hypermobility involves an increased range of motion compared to normal amplitudes for the same age, sex and ethnic group. Patients with hypermobility suffer from joints problems and ... [more ▼]. Introduction: Joint hypermobility involves an increased range of motion compared to normal amplitudes for the same age, sex and ethnic group. Patients with hypermobility suffer from joints problems and chronic pain is the most frequently reported symptom. Eccentric muscle strengthening could be very important to protect hypermobile joints. Case report: An Ehler-Danlos syndrome patient presented pain in the right elbow and the right wrist after a season of tennis. Her physiotherapy (18 sessions, 3 times a week) consisted of wrist prono-supination and flexion-extension muscle group reinforcement and proprioceptive training. To protect the wrist against excessive load, the eccentric strengthening exercises of prono-supinator and ...

In November of 2014, I was diagnosed with EDS-Hypermobility type. There are many diagnostic criteria for this type of EDS, which I wont go into detail about here. The reason there are a number of criteria is because EDS is a connective tissue disorder that affects each person differently. One of the diagnostic criteria, alongside family history, symptoms & a number of other things is the Beighton scale. This is a scale whereby certain joints are tested for their flexibility. At this appointment, I scored a 9/9. Frustratingly, not all joints are covered by this scale (like the hips - one of my most flexible areas) This is another reason why the Beighton scale is just one of the things used to diagnose EDS-Hypermobility type. I was sent for a course of physio with a senior therapist who specialised in connective tissue disorders, which proved very helpful. This physio helped with physical supports to make it possible for me to play my oboe again. ...

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Hansard (the Official Report) is the edited verbatim report of proceedings of both the House of Commons and the House of Lords. Daily Debates from Hansard are published on this website the next working day.

Double-what-ted? Hypermobility - Hypermobility lets you contort your body in unusual ways. Learn if you can really be double-jointed and how that relates to hypermobility.

Its amazing to watch a contortionist turn into a human pretzel. But for most of us hyper-extending joints and overstretching already loose connective ...

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I walked into consultants room and he said hypermobile and marfens before I had even sat down. Checked skin, Beighton scale and had a chat and he said we will do a few tests but I suspect Ehlers-Danlos. Looked at my medical history and said definitely pots but we will check you for vascular too as family history points towards a pattern of heart issues and also sound eds too but obviously havent had diagnosis. He said it was all too easy to connect the dots at that point and its important now that type is identified quickly so that we can predict or treat quickly any problems that arise in the future. Said cardiologist will check for vascular as some markers in Bloods were concerning but not obvious if its pointing towards vascular or separate problem and that the departments will work together to ensure that Im getting the help I need but said at the end of the day theres not a huge amount they can do and its all about finding the right way to deal with things and pushing on.. I was ...

Joint hypermobility is a spectrum of disorders that affects the suppleness of joints making them unusually flexible and is often referred to as double-jointedness.

HYPERTENSION and JOINT LAXITY related symptoms, diseases, and genetic alterations. Get the complete information with our medical search engine for phe

I got my wheelchair a year ago last January and I should have gotten one many years before that! I had no idea how helpful it would be on so many levels. At my worst I was able to use it from the bedroom to the bathroom -- which was the only two places I was going at the time. I use my chair now only when I leave the house, which admittedly I am still too sick to do very often. But I absolutely love doing for a stroll around the cul dsac on my own power. My arms are strong and it feels so good to work my upper body in the chair. I found that I did far more exercise with my chair than I ...

Supermarket assistant Ashleigh Alqotaibi, 22, from Beighton, Sheffield, started losing her hair due to stress because of an unhappy relationship but after meeting her fiance John Robinson.

O Adewumi, B Aflatoonian, L Ahrlund-Richter, M Amit, PW Andrews, G Beighton, PA Bello, N Benvenisty, LS Berry, S Bevan, B Blum, J Brooking, KG Chen, AB Choo, GA Churchill, M Corbel, I Damjanov, JS Draper, P Dvorak, K Emanuelsson, RA Fleck, A Ford, K Gertow, M Gertsenstein, PJ Gokhale, RS Hamilton, A Hampl, LE Healy, O Hovatta, J Hyllner, MP Imreh, J Itskovitz-Eldor, J Jackson, JL Johnson, M Jones, K Kee, BL King, BB Knowles, M Lako, F Lebrin, BS Mallon, D Manning, Y Mayshar, RD McKay, AE Michalska, M Mikkola, M Mileikovsky, SL Minger, HD Moore, CL Mummery, A Nagy, N Nakatsuji, CM OBrien, SK Oh, C Olsson, T Otonkoski, KY Park, R Passier, H Patel, M Patel, R Pedersen, MF Pera, MS Piekarczyk, RA Pera, BE Reubinoff, AJ Robins, J Rossant, P Rugg-Gunn, TC Schulz, H Semb, ES Sherrer, H Siemen, GN Stacey, M Stojkovic, H Suemori, J Szatkiewicz, T Turetsky, T Tuuri, S van den Brink, K Vintersten, S Vuoristo, D Ward, TA Weaver, LA Young, W Zhang The International Stem Cell Initiative characterized 59 ...

Learn how to control pain from hypermobility from two physical therapists who live and work with hypermobility everyday. Were here to teach you how to live life with less pain. Its all about how you do things, not giving up on them.

Structures of thin films bonded on thick substrates are abundant in biological systems and engineering applications. Mismatch strains due to expansion of the films or shrinkage of the substrates can induce various modes of surface instabilities such as wrinkling, creasing, period doubling, folding, ridging, and delamination. In many cases, the film-substrate structures are not flat but curved. While it is known that the surface instabilities can be controlled by film-substrate mechanical properties, adhesion and mismatch strain, effects of the structures curvature on multiple modes of instabilities have not been well understood. In this paper, we provide a systematic study on the formation of multimodal surface instabilities on film-substrate tubular structures with different curvatures through combined theoretical analysis and numerical simulation. We first introduce a method to quantitatively categorize various instability patterns by analyzing their wave frequencies using fast Fourier ...

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What happens to our face when we age? As we age, skin loses elasticity and tension. Soft tissue descends due to a combination of ligament laxity and gravity. All these contribute to sagginess in our laugh lines, jawlines and eyelids. What is Korean HIFU vs Ulthera vs Thermage? HIFU refers to high intensity focused ultrasound.…

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An old-fashioned way to describe people with joint hypermobility, from the notion that their fingers and limbs could bend so far that there must be a se...

HIPERMOVILIDAD ARTICULAR PDF - Abstract. SUAREZ AYALA, Diana Vanessa; VALENCIA, María and GOMEZ MORA, María del Pilar. Relationship between generalised joint hypermobility and .

Joint EDS UK and HMSA response to the British Society of Rheumatology Guidance for Management of Symptomatic Hypermobility in Children and Young People - A Guide for Professionals managing Children and Young People with this condition

hi ladies, beeen a while, computer was poorly!! anyway will get straight to my rant cos i am livid!! my dd now 4 has hypermobility amongst other things as yet undiagnosed(still)!! lshe always falls a lot, & nursery commented about it as well, physio came out & said muscles little weak in ankles

Hypermobility, often termed double jointed, is a common health condition among children and adults. Strengthening your joints can help make this manageable.

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Gosh you sound EXACTLY like me! And your little ones list is identical to mine lol. So I think we are the norm and our babies are just right! I highly doubt any baby at 6 months is trying to walk! I guess Ive heard of it but that is so super rare and if I havent seen it with my own eyes then I call bull lol. I think the same things all the time with mine, is he behind? is he just lazy? is he going to all of a sudden do a bunch of new things at one time? But, it all comes down to they all go at their own pace. My first son did not sit unassisted until 7 1/2 months, he NEVER crawled and only scooted on his bottom, he did not walk until 18 months (this was due to hypermobile joints and PT helped right away). This little guy who turned 6 months on Oct 3rd still does not sit but for a few seconds at a time, nowhere near crawling, doesnt even get up on his knees, babbles loudly and the bababababa or dadadada are not words, they are babble lol! He rolls only when he feels like it but not ...

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