Schizencephaly in triple-X syndrome

Pediatrics International

Volumn 43, Issue 3, 2001, Pages 296-297

  Ehara, Hiroaki ^a,c   Eda, Isematsu ^b  

^a TOTTORI UNIVERSITY   (Japan)

^b Department of Pediatrics   (Japan)

^c TOTTORI UNIVERSITY   (Japan)

Author keywords

Schizencephaly; Superfemale; Triple X syndrome

Indexed keywords

ANTICONVULSIVE AGENT;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CLINICAL FEATURE; ELECTROENCEPHALOGRAM; EPILEPSY; FEMALE; HUMAN; KARYOTYPE 47,XXX; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SCHIZENCEPHALY;

ADULT; BRAIN; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; SEX CHROMOSOME ABERRATIONS; TRISOMY; X CHROMOSOME;

EID: 0034932369     PISSN: 13288067     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1442-200X.2001.01382.x     Document Type: Article

References (11)

1. The triplo-X female: An appraisal based on a study of 12 cases and a review of the literature
2. Intelligence and achievement in children with extra X aneuploidy: A longitudinal perspective
3. Trisomy X: ACLF (Association des Cytogénéticiens de Langue Française) retrospective study
4. Developmental malformations produced by radiation: A timetable of their development
5. Formation, maturation, and disorders of brain neocortex
6. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats
7. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
8. Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
9. Schizencephaly: Correlations of clinical and radiologic features
10. The frequency of chromosome abnormalities detected in consecutive newborn studies: Differences between studies. Results by sex and by severity of phenotypic involvement
11. Schizencephaly: A clinical and CT study