Partial albinism, immunodeficiency, hypergammaglobulinemia and Dandy-Walker cyst--a Griscelli syndrome variant.
Indian Pediatr
;
2003 Oct; 40(10): 1005-8
Artigo
em Inglês
| IMSEAR
| ID: sea-13377
ABSTRACT
A 6-year-old girl presented with recurrent infections, seizures, regression of milestones, silvery hair and organomegaly. A diagnosis of Griscelli syndrome with unusual features of a Dandy Walker cyst and hypergammaglobulinemia, not previously described in literature, was made. The child was treated with supportive measures.
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Assunto principal:
Síndrome
/
Feminino
/
Humanos
/
Criança
/
Piebaldismo
/
Síndrome de Dandy-Walker
/
Hipergamaglobulinemia
/
Síndromes de Imunodeficiência
Idioma:
Inglês
Revista:
Indian Pediatr
Ano de publicação:
2003
Tipo de documento:
Artigo
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