Hereditary Tyrosinemia Type 1-A Rare Disease with Typical Radiological Features: Case Report and Review of Literature

Hereditary tyrosinemia type 1 is one of the many inborn errors of metabolism associated with tyrosine catabolism. It is a rare disease with its incidence or prevalence in India unknown. The cascading alternate metabolism results in characteristic injury patterns to the liver, kidneys, and the centra...

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Main Authors: Somesh Singh (Author), Rana Vishwadeep Mall (Author), Pragya Chaturvedi (Author), Rajnikant R. Yadav (Author)
格式: 圖書
出版: Thieme Medical and Scientific Publishers Pvt. Ltd., 2020-05-01T00:00:00Z.
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索引號: A1234.567
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