Cargando…
High incidence of null variants identified from newborn screening of X-linked adrenoleukodystrophy in Taiwan
BACKGROUND: Adrenoleukodystrophy (ALD) is an X-linked peroxisomal disorder caused by variants in the ABCD1 gene and can lead to Addison disease, childhood cerebral ALD, or adrenomyeloneuropathy. Presymptomatic hematopoietic stem cell transplantation is the only curative treatment for the disease and...
Autores principales: | Chen, Hui-An, Hsu, Rai-Hseng, Chen, Pin-Wen, Lee, Ni-Chung, Chiu, Pao-Chin, Hwu, Wuh-Liang, Chien, Yin-Hsiu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421440/ https://www.ncbi.nlm.nih.gov/pubmed/36046390 http://dx.doi.org/10.1016/j.ymgmr.2022.100902 |
Ejemplares similares
-
Aromatic l‐amino acid decarboxylase deficiency in Taiwan
por: Hwu, Wuh‐Liang, et al.
Publicado: (2023) -
Duchenne muscular dystrophy newborn screening: the first 50,000 newborns screened in Taiwan
por: Chien, Yin-Hsiu, et al.
Publicado: (2022) -
Asymptomatic ASS1 carriers with high blood citrulline levels
por: Chen, Hui‐An, et al.
Publicado: (2022) -
The Timely Needs for Infantile Onset Pompe Disease Newborn Screening—Practice in Taiwan
por: Chiang, Shu-Chuan, et al.
Publicado: (2020) -
Late-onset symptomatic hyperprolactinemia in 6-pyruvoyl-tetrahydropterin synthase deficiency
por: Hsu, Rai-Hseng, et al.
Publicado: (2023)