Cholestasis and hypercalcemia secondary to panhypopituitarism in a newborn.
Turk J Pediatr
; 59(1): 100-103, 2017.
Article
em En
| MEDLINE
| ID: mdl-29168375
ABSTRACT
Dursun F, Gerenli N, Kirmizibekmez H. Cholestasis and hypercalcemia secondary to panhypopituitarism in a newborn. Turk J Pediatr 2017; 59 100-103. Cholestatic hepatitis and hypercalcemia are rare features of hypopituitarism in newborns. So diagnosis of hypopituitarism is frequently delayed. The most frequent symptoms of congenital hypopituitarism are hypoglycemia, prolonged jaundince and micropenis. A patient with congenital hypopituitarism associated with cholestasis and hypercalcemia is reported here. Newborns with hypercalcemia and cholestasis should alert pediatricians to the possibility of congenital hypopituitarism and prompt endocrinological investigation.
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Texto completo:
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Base de dados:
MEDLINE
Assunto principal:
Colestase
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Terapia de Reposição Hormonal
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Hipercalcemia
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Hipopituitarismo
Idioma:
En
Ano de publicação:
2017
Tipo de documento:
Article