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Updated: Jul 30, 2025

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Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
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Novel Mutation of Tyrosinemia in a Child With Hypophosphatemic Rickets
Surabhi Dogra1, Karunesh Kumar1, Rohan Malik2,3
1From the Department of Pediatric Gastroenterology, Indraprastha Apollo Hospital, New Delhi, India.
JPGN Reports
|May 11, 2023
Abstract:
Tyrosinemia is an inherited metabolic disease of fumarylacetoacetate enzyme. A male infant presented to us with clinical features of rickets, floppiness, and a deranged coagulation profile. A novel mutation causing Tyrosinemia was discovered on the basis of genetic sequencing.
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