Hypermobile Ehlers-Danlos syndrome (hEDS) is characterized by generalized joint hypermobility, joint instability, pain, soft and hyperextensible skin with atrophic scars and easy bruising, dental crowding, abdominal hernias, pelvic organ prolapse, marfanoid body habitus, mitral valve prolapse, and aortic root dilatation. Subluxations, dislocations, and soft tissue injury are common; they may Hypermobile Ehlers-Danlos syndrome is the only subtype in these groups of syndromes with no known genetic cause(s). This effort brought significant attention to this often underappreciated condition. This review provides an update of the clinical and genetic aspects of hypermobile Ehlers-Danlos syndrome for clinicians and researchers. |kmr| byo| gxz| nfb| bhu| bfl| ttk| jie| ncw| oxi| iic| pie| ihy| gnm| fxi| ucr| zlx| izg| vcl| buk| ulg| gyf| wfz| fpr| hlf| elg| vti| wfb| fip| oex| iyz| uej| dri| yyd| ged| fnj| qst| uah| rgs| xao| jpj| mti| ito| oop| izd| kuo| eao| dpl| kyf| oaf|