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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...
Autores principales: | Aldossari, Shaikha, Al Bakri, Amani, Kamal, Yumna |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
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 |
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