Neonatal Hypopituitarism: Unusual Presentation

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Neonatal Hypopituitarism: Unusual Presentation

Congenital hypopituitarism is a rare condition associated with possible serious complications and long-term neurological sequelae, if not promptly recognized and treated.1 Neonates with congenital hypopituitarism may present with or without associated developmental defects, such as ocular, midline, and genital abnormalities. They may also present with nonspecific symptoms, including hypoglycemi...

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Optic nerve hypoplasia with hypopituitarism and intact septum pellucidum is a variant of septo-optic dysplasia or deMorsier's syndrome.' Although neonatal jaundice has been seen with this syndrome, the association with severe prolonged cholestatic jaundice has not been emphasised. We describe three patients who presented with cholestatic jaundice and were found to have optic nerve hypoplasia an...

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Neonatal cholestasis and hypopituitarism.

We read with interest the paper by Kaufman et al' on neonatal cholestasis and hypopituitarism. We have been treating a similar patient whose problems were complicated by diabetes insipidus of pituitary origin. She was referred from another hospital at the age of 1 month for assessment of secondary hypothyroidism, cholestatic jaundice, temperature instability, and microcephaly. She was born at 4...

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An unusual case of hypopituitarism.

A 14-year-old boy presented to the trauma unit at our tertiary hospital after sustaining a gunshot wound to the left eye. Clinical examination showed that he was alert and haemodynamically stable, but blind in the left eye, with no CSF rhinorrhoea. His pubertal status (Tanner stage S3) and height (1·7 m, 75th percentile) were appropriate for his chronological age. Skull radiography and a CT sca...

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ژورنال

عنوان ژورنال: Journal of Child Science

سال: 2017

ISSN: 2474-5871

DOI: 10.1055/s-0037-1604449