Clinical, Biochemical, and Molecular Characteristics of Filipino Patients with Tyrosinemia Type 1

Hereditary tyrosinemia type I (HT1), or hepatorenal tyrosinemia, is an amino acid disorder which may cause hepatic failure as well as renal and neurologic comorbidities. Early detection of this disorder is possible with newborn screening (NBS). The objective of this study is to describe the clinical...

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Номзүйн дэлгэрэнгүй

Үндсэн зохиолчид:	Barbra Charina V. Cavan, Leniza G. de Castro-Hamoy, Conchita G. Abarquez, Ebner Bon G. Maceda, Maria Melanie Liberty B. Alcausin
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	MDPI AG 2024-08-01
Цуврал:	International Journal of Neonatal Screening
Нөхцлүүд:	tyrosinemia type I hepatorenal tyrosinemia expanded newborn screening
Онлайн хандалт:	https://www.mdpi.com/2409-515X/10/3/59
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!