A Case of Type II Ehlers-Danlos Syndrome / 대한피부과학회지
Korean Journal of Dermatology
;
: 997-998, 2000.
Artigo
em Coreano
| WPRIM
| ID: wpr-205589
ABSTRACT
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 different 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 hyperextensibility, thin atrophic scarring from trauma, and hypermobile finger joints.
Texto completo:
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Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Pele
/
Cicatriz
/
Tecido Conjuntivo
/
Síndrome de Ehlers-Danlos
/
Articulações dos Dedos
/
Articulações
/
Biologia Molecular
/
Manifestações Neurológicas
Limite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Ano de publicação:
2000
Tipo de documento:
Artigo
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