遗传性阻塞性睡眠呼吸暂停(OSA)与EDS相关。 另可伴慢性疼痛(chronic pain)、自主神经异常(dysautonomia)、胃肠道运动失调(gastrointestinal dysmotility)、肥大细胞激活(mast cell activation)、焦虑(anxiety)、恐惧症(phobic states)。 放射学可见钙质沉积。 (消化道症状) 5诊断 依据临床表现多可临床诊断EDS。基因筛查可...
[9]EMMANOUIL G,JEFFREY RB,JOHN PD,et al.Postural orthostatic tachycardia syndrome(POTS):Association with Ehlers-Danlos syndrome and Orthopaedic considerations[J].Clin Orthop Relat Res, 2015,473:722-728.[10]GAZIT Y,NAHIR AM,GRAHAME R,et al.Dysautonomia in the joint hypermobility syndrome[J].Am...
Dysautonomia and its underlying mechanisms in the hypermobility type of Ehlers- Danlos syndrome. Semin Arthritis Rheum. 2014;44:93-100De Wandele I, Rombaut L, Leybaert L, et al. Dysautonomia and its underlying mechanisms in the hypermobility type of Ehlers-Danlos syndrome. Semin Arthritis ...
Ehlers-Danlos Syndrome (EDS) comprises a heterogeneous group of diseases characterized by joint hypermobility, connective tissue friability, and vascular fragility. Reliable prognostic factors predicting vascular disease progression (e.g. arterial aneurysms, dissections, and ruptures) in EDS patients are ...
We retrospectively analyzed electronic medical records of patients with Ehlers-Danlos Syndrome hypermobility type (HEDS), including demographic information, workup, rheumatological diagnoses in order to determine its association with rheumatological cond
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PART THREE: PROBLEMS, PREVALENCE AND RISK FACTORS 5.0 What Can Cause Ehlers-Danlos Syndromes? EDS can be caused by: Being generally inherited through two known inheritance patterns:Autosomal Dominant (AD): If you get the abnormal gene from only one paren
(due to damage to unstable joints), dysautonomia, gastrointestinal dysmotility, mast cell activation (allergies,asthma, etc), andanxietyand phobias. Serious complications, such as vascular or organ rupture, have been reported in vascular and kyphoscoliotic EDS, but all types of EDS should be ...
POTS is a syndrome of dysautonomia, characterised by multiple symptoms, many of which occur on postural change or standing. These include transient loss of consciousness, presyncope, dizziness, palpitations, chest pain and shortness of breath. In patients with the autosomal recessive condition of ...
The diagnosis was based on actual or previous hypermobility, joint instability, chronic pain, skin abnormalities and several other criteria as chronic fatigue, proprioceptive disorders, dysautonomia, migraines, digestive disorders. Almost all patients had a family history of hEDS with variability in ...