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Congenital hypopituitarism associated with hyperammonemia.
Indian J Pediatr ; 2009 Mar; 76(3): 327-8
Article in English | IMSEAR | ID: sea-81111
ABSTRACT
Neonatal onset hypopituitarism is a life threatening but potentially treatable metabolic condition. However, in the majority of cases it can be fatal due to the metabolic disturbances. We report a newborn with profound symptomatic hypoglycemia and hyperammonemia who initially was thought to have an inborn error of metabolism (IEM). After an initial falsely reassuring magnetic resonance imaging (MRI) brain scan, further endocrine investigation eventually led to the correct diagnosis and treatment.
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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pituitary Gland / Thyroxine / Female / Humans / Infant, Newborn / Magnetic Resonance Imaging / Treatment Outcome / Hormone Replacement Therapy / Hyperammonemia / Diagnosis, Differential Type of study: Diagnostic study Language: English Journal: Indian J Pediatr Year: 2009 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pituitary Gland / Thyroxine / Female / Humans / Infant, Newborn / Magnetic Resonance Imaging / Treatment Outcome / Hormone Replacement Therapy / Hyperammonemia / Diagnosis, Differential Type of study: Diagnostic study Language: English Journal: Indian J Pediatr Year: 2009 Type: Article