Chorea-acanthocytosis: A Case Report with Review of Oral Manifestations

Chorea-acanthocytosis (ChAc) is an autosomal recessive, progressive neurological disorder due to mutation in VPS13A gene causing defects in sorting of protein making the cell membrane unstable, leading to star-shaped erythrocytes. This neurological disorder includes features such as elevated creatin...

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Detalles Bibliográficos
Autores principales: Urs, Aadithya B., Augustine, Jeyaseelan, Khan, Azhar Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092098/
https://www.ncbi.nlm.nih.gov/pubmed/33967542
http://dx.doi.org/10.4103/ccd.ccd_207_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092098/
https://www.ncbi.nlm.nih.gov/pubmed/33967542
http://dx.doi.org/10.4103/ccd.ccd_207_20

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