Home > Journals > Minerva Pediatrica > Past Issues > Minerva Pediatrica 2009 August;61(4) > Minerva Pediatrica 2009 August;61(4):441-4

CURRENT ISSUE
 

JOURNAL TOOLS

eTOC
To subscribe
Submit an article
Recommend to your librarian
 

ARTICLE TOOLS

Reprints
Permissions

 

CASE REPORTS   

Minerva Pediatrica 2009 August;61(4):441-4

Copyright © 2009 EDIZIONI MINERVA MEDICA

language: Italian

Arachnoid cyst, hypoplasic temporal lobe and facial anomalies: a neurocristopathy

Berio A., Piazzi A.

Dipartimento di Scienze Pediatriche “G. De Toni”, Cattedra di Pediatria dell’Università di Genova, Genova, Italia


PDF


The authors report on a patient which presented at birth facial anomalies similar to those of facial alcoholic syndrome (i.e. high forehead, wide nasal bridge, upturned nose, flat philtrum), low set ears, short neck. Successive-ly, also an arachnoide right temporo-polar cyst with hypoplasic right temporal lobe was diagnosed. They think that cerebral cyst, hypoplastic temporal lobe and facial anomalies are congenital. By the origin of facial and leptomeningeal structures from the neural crests, the authors conclude that facial, arachnoid and cerebral anomalies depend from the derangement of the neural crest development and that this complex syndrome is a neurocristopathy which can be ascribed to dysneurulation.

top of page