Hereditary Tyrosinemia Type 1 in Jordan: A Retrospective Study.
Noor A MegdadiAhmad K AlmigdadMo'men O AlakilShahrazad M AlqiamSumaia G RababahMoshera A DwiariPublished in: International journal of pediatrics (2021)
HT1 diagnosis is usually delayed because it is not part of newborn screening and nonfamiliarity with the clinical features of the disease. Therefore, nationwide newborn screening should be expanded to include HT1.
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