Crouzon syndrome with acanthosis nigricans: a case report and literature review

Crouzon syndrome with acanthosis nigricans is an autosomal dominant disease, with typical features of classic Crouzon craniosynostosis, verrucous hyperplasia, and hyperpigmentation of the skin. While several mutations in FGFR2 cause classic Crouzon syndrome, Crouzon syndrome with acanthosis nigrican...

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Detalles Bibliográficos
Autores principales: Nguyen, Quan Duy, Tran, Tu Nguyen Anh, Nguyen, Hao Trong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312108/
https://www.ncbi.nlm.nih.gov/pubmed/37397405
http://dx.doi.org/10.4081/dr.2023.9620

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312108/
https://www.ncbi.nlm.nih.gov/pubmed/37397405
http://dx.doi.org/10.4081/dr.2023.9620

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