A special case of congenital adrenal hypoplasia and acute bilateral infantile striatal necrosis.
Acta Paediatr
; 84(8): 957-60, 1995 Aug.
Article
em En
| MEDLINE
| ID: mdl-7488830
ABSTRACT
Isolated mineralocorticoid deficiency is described in a 5-week-old boy. The deficiency progressed to general adrenal insufficiency during the boy's first year of life. The family history suggested X-linked inheritance. At 18 months of age the patient developed acute bilateral infantile striatal necrosis, which might suggest a possible relationship between both entities.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Insuficiência Adrenal
/
Corpo Estriado
Tipo de estudo:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
Limite:
Child, preschool
/
Humans
/
Infant
/
Male
Idioma:
En
Ano de publicação:
1995
Tipo de documento:
Article