Griscelli syndrome - a case report.
Indian Pediatr
;
2004 Jul; 41(7): 734-7
Artículo
en Inglés
| IMSEAR
| ID: sea-15816
ABSTRACT
Griscelli syndrome is a rare autosomal recessive disorder characterized by partial albinism with variable immunodeficiency. Silvery gray hair with large, clumped melanosomes on microscopy of hair shafts are diagnostic. The commonest complication leading to mortality includes lymphohistiocytic proliferation in various organs, including the brain. We present a child with classic clinical features and confirmatory findings of clumped melanosomes on microscopy of hair shaft.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Síndrome
/
Femenino
/
Humanos
/
Piebaldismo
/
Inmunodeficiencia Variable Común
/
Resultado Fatal
/
Lactante
Idioma:
Inglés
Revista:
Indian Pediatr
Año:
2004
Tipo del documento:
Artículo
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