A rare case of primary congenital glaucoma in combination with neurofibromatosis 1: a case report

BACKGROUND: Neurofibromatosis 1 (NF1) is a common disease that mainly affects the skin and peripheral nervous system, and is characterized by bony dysplasia. Primary congenital glaucoma (PCG) is a sight-threatening disease that can manifest as a prodrome of NF1, especially in newborn babies. We repo...

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Detalles Bibliográficos
Autores principales: Li, Haijun, Liu, Ting, Chen, Xia, Xie, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625924/
https://www.ncbi.nlm.nih.gov/pubmed/26514695
http://dx.doi.org/10.1186/s12886-015-0142-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625924/
https://www.ncbi.nlm.nih.gov/pubmed/26514695
http://dx.doi.org/10.1186/s12886-015-0142-8

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