Adequacy of nitisinone for the management of alkaptonuria

Alkaptonuria is a rare hereditary disease with a defective enzyme that results in increased homogentisic acid levels in the body. Homogentisic acid accumulates in multiple body parts and initializes tissue damage. Clinical manifestations such as pigmentation of the skin areas and joint destruction r...

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Detalles Bibliográficos
Autores principales: Abbas, Khawar, Basit, Jawad, Rehman, Mohammad Ebad ur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9422360/
https://www.ncbi.nlm.nih.gov/pubmed/36045846
http://dx.doi.org/10.1016/j.amsu.2022.104340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9422360/
https://www.ncbi.nlm.nih.gov/pubmed/36045846
http://dx.doi.org/10.1016/j.amsu.2022.104340

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