Published 1998 | Version v1
Journal article

Joubert syndrome

  • 1. Hospital Senora de Aranzazu. San Sebastian (Spain)

Description

Joubert syndrome is a rare malformation of the posterior fossa, mainly affecting the cerebellar vermis, which generally appears as a dysplastic lesion. Other structures of the cervico medullary junction may be involved, with accompanying brainstem hypoplasia according to neuroimaging studies. The diagnosis is usually reached during, childhood, based on a constellation of changes in the child's neurological development that are supported by the results of imaging studied. Respiratory problems are the most common signs in newborns,leading to the suspicion of the presence of this syndrome. (Author) 11 refs

Additional details

Additional titles

Original title (Spanish)
Sindrome de Joubert

Publishing Information

Journal Title
Radiologia (Madrid)
Journal Volume
40
Journal Issue
8
Journal Page Range
p. 536-539
CODEN
RBSEBR

INIS

Country of Publication
Spain
Country of Input or Organization
Spain
INIS RN
30010074
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
COMPUTERIZED TOMOGRAPHY; DIAGNOSIS; MAGNETIC RESONANCE; MALFORMATIONS; NERVOUS SYSTEM
Descriptors DEC
DISEASES; PATHOLOGICAL CHANGES; RESONANCE; TOMOGRAPHY