Werner syndrome: a case report and review of literature
JPAD-Journal of Pakistan Association of Dermatologists. 2011; 21 (4): 304-308
en Inglés
| IMEMR
| ID: emr-118221
ABSTRACT
Werner's syndrome is a rare inherited disorder characterized by short stature, sclerosed skin, cataract and premature aging of the face. The disease involves multiple systems of the body and some of the abnormalities may cause life threatening complications such as myocardial infarction and malignancy. We report a case of this rare disorder
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Progeria
/
Síndrome de Werner
/
Síndrome de Cockayne
/
Envejecimiento Prematuro
Tipo de estudio:
Informe de Casos
Límite:
Adulto
/
Humanos
/
Masculino
Idioma:
Inglés
Revista:
J. Pak. Assoc. Dermatol.
Año:
2011
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