A rare variation of hydranencephaly: case report

Hydranencephaly is a rare congenital abnormality characterized by the absence and replacement of the cerebral hemispheres with cerebrospinal fluid. Here, we present an ultrasonographic diagnosis of a case of a rare variant of fetal hydranencephaly at 38 weeks of gestation. Obstetric sonography revea...

Descripción completa

Detalles Bibliográficos
Autores principales: Wijerathne, Buddhika TB, Rathnayake, Geetha K, Ranaraja, Sisira K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945765/
https://www.ncbi.nlm.nih.gov/pubmed/24627761
http://dx.doi.org/10.12688/f1000research.1-22.v3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945765/
https://www.ncbi.nlm.nih.gov/pubmed/24627761
http://dx.doi.org/10.12688/f1000research.1-22.v3

Ejemplares similares