Primary hyperoxaluria type 1 with a novel mutation.

[primary hyperoxaluria type 1]

Primary hyperoxaluria type 1 [PH 1 ] is an autosomal recessive disorder caused by a deficiency of alanine-glyoxylate aminotransferase AGT , which is encoded by the AGXT gene . We report an Indian family with two affected siblings having a novel mutation in the AGXT gene inherited from the parents . The index case progressed to end stage renal disease at 5 months of age . His 4 month old sibling is presently under follow up with preserved renal function .

Diseases
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Diseases presenting "mutation in the agxt gene" symptom

primary hyperoxaluria type 1

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