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: | , , , |
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| Format: | Book |
| Published: |
Thieme Medical and Scientific Publishers Pvt. Ltd.,
2020-05-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |