Arnold-Chiari Malformation Type II and CYP1B1 Congenital Glaucoma: A Possible Association

BACKGROUND: We describe a case of an infant with Arnold-Chiari Malformation Type II (ACM-II) who was born with lumbosacral myelomeningocele, hydrocephalus, and primary congenital glaucoma (PCG) together with dysmorphic features (scaphocephaly, frontal bossing, hypotelorism, entropion, and flat nasal...

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Detalles Bibliográficos
Autores principales: Aldossari, Shaikha, Al Bakri, Amani, Kamal, Yumna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478586/
https://www.ncbi.nlm.nih.gov/pubmed/34594583
http://dx.doi.org/10.1155/2021/4808346

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478586/
https://www.ncbi.nlm.nih.gov/pubmed/34594583
http://dx.doi.org/10.1155/2021/4808346

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