Joubert syndrome with associated corpus callosum agenesis

European Journal of Paediatric Neurology

Volumn 6, Issue 1, 2002, Pages 63-66

  Zamponi, N ^a   Rossi, B ^a   Messori, A ^b   Polonara, G ^b   Regnicolo, L ^b   Cardinali, C ^a  

^a Ospedale Pediatrico G Salesi   (Italy)

^b UNIVERSITÀ POLITECNICA DELLE MARCHE   (Italy)

Author keywords

Corpus callosum agenesis; Joubert syndrome; Magnetic resonance imaging; Psychomotor delay

Indexed keywords

APNEA; ARTICLE; ATAXIA; BRAIN REGION; CASE REPORT; CEREBELLUM VERMIS; CLINICAL FEATURE; CORPUS CALLOSUM AGENESIS; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DISEASE SEVERITY; EYE MOVEMENT DISORDER; FAMILY; FEMALE; HUMAN; HYPERPNEA; HYPOTHESIS; INFANT; JOUBERT SYNDROME; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER;

EID: 0036224347     PISSN: 10903798     EISSN: None     Source Type: Journal    
DOI: 10.1053/ejpn.2001.0542     Document Type: Article

References (6)

1. Familial agenesis of the cerebellar vermis: A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation
2. Clinical features and revised diagnostic criteria in Joubert syndrome
3. Autism and autistic behavior in Joubert syndrome
4. Magnetic resonance imaging features and classification of central nervous system malformation in Joubert syndrome
5. Neuropathology of Joubert syndrome
6. Neurobehavioral development in Joubert syndrome