Uncombable Hair in a Case of Zellweger Syndrome – A New Association

Zellweger syndrome (ZS) is a rare autosomal recessive, peroxisomal biogenesis disorder (PBD) that occurs due to a mutation in any of the thirteen peroxin (PEX) genes. It is reported to manifest with varying degrees of severity, ranging from non-specific gastrointestinal abnormalities, nail and ename...

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Detalles Bibliográficos
Autores principales: Jahnavi, Yatham, Sharada, R. G, Wahab, Afthab Jameela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10231715/
https://www.ncbi.nlm.nih.gov/pubmed/37266105
http://dx.doi.org/10.4103/idoj.idoj_467_22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10231715/
https://www.ncbi.nlm.nih.gov/pubmed/37266105
http://dx.doi.org/10.4103/idoj.idoj_467_22

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