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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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI AG
2024-08-01
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| coleção: | International Journal of Neonatal Screening |
| Assuntos: | |
| Acesso em linha: | https://www.mdpi.com/2409-515X/10/3/59 |
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