Septo-optic dysplasia with amniotic band syndrome sequence: a case report

INTRODUCTION: De Morsier syndrome, or septo-optic dysplasia, is a rare, heterogeneous, complex condition with a highly variable phenotype. It is characterized by optic nerve hypoplasia, pituitary gland hypoplasia, and midline brain abnormalities, including absence of septum pellucidum and corpus cal...

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Detalles Bibliográficos
Autores principales: Amiji, Insiyah A., Mohamed, Ummulkheir H., Rutashobya, Adelina G., Mngoya, Mariam, Schoenmann, Nicole, Naburi, Helga E., Manji, Karim P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913001/
https://www.ncbi.nlm.nih.gov/pubmed/31839004
http://dx.doi.org/10.1186/s13256-019-2306-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913001/
https://www.ncbi.nlm.nih.gov/pubmed/31839004
http://dx.doi.org/10.1186/s13256-019-2306-2

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