대피지
2000:38:7 997-999
Ehlers-Danlos
syndrome is a heterogeneous group of inherited generalized connective tissue disorders
characterized by hyperextensibility and fragility of skin, joint hepermobility,
abnormal scarring, easy bruisibility, visceral and neurological manifestations.
It is classified into 10 differente major subtypes based on genetic, biochemical,
and clinical characteristics. We report a case of type Ⅱ Ehlers-Danlos syndrome
in a 19-year-old male who showed soft and velvety skin with marked hyperestensibility,
thin atrophic scarring from trauma, and hypermobile finger joints. |
