1.
Indian Pediatr
;
2005 Feb; 42(2): 173-4
Artigo
em Inglês
| IMSEAR
| ID: sea-10648
RESUMO
This report describes a male baby with primary hyperoxaluria type-1, presenting at 5 hours of age with cyanotic episodes, hypotonia, unexplained techypnea and tachycardia. This infant also had renal calcinosis, and middle cerebral arterial infarct with unilateral enlargement of ventricle and left porencephalic cyst on CT scan. The infant improved with diuretics, water supplementation, pyridoxine, and Albright solution.