Toriello-Carey syndrome: Evidence for X-linked inheritance

American Journal of Medical Genetics

Volumn 65, Issue 4, 1996, Pages 291-294

  Czarnecki, Paula ^a   Lacombe, Didier ^b   Weiss, Lester ^a,c  

^a HENRY FORD HOSPITAL   (United States)

^b Children s Hospital   (France)

^c Ford Hospital   (United States)

Author keywords

agenesis of the corpus callosum; cardiac defect; developmental delay; malformed ears; Robin sequence; X linked

Indexed keywords

ARTICLE; CASE REPORT; CONGENITAL HEART MALFORMATION; CORPUS CALLOSUM AGENESIS; DEVELOPMENTAL DISORDER; EAR MALFORMATION; HUMAN; INFANT; MALE; MUSCLE HYPOTONIA; NEWBORN; PALPEBRAL FISSURE ANOMALY; PIERRE ROBIN SYNDROME; PRIORITY JOURNAL; TELECANTHUS; TORIELLO CAREY SYNDROME; X CHROMOSOMAL INHERITANCE;

ABNORMALITIES, MULTIPLE; BRAIN; FEMALE; GROWTH DISORDERS; HUMANS; INFANT; INFANT, NEWBORN; MAGNETIC RESONANCE IMAGING; MALE; SYNDROME; X CHROMOSOME;

ERETMOCHELYS IMBRICATA; GENETTA;

EID: 0029852706     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961111)65:4<291::AID-AJMG9>3.0.CO;2-S     Document Type: Article

References (4)

1. Camera G, Righi E, Romagnoli G (1993): Toriello-Carey syndrome: Report of a new case. Clin Dysmorphol 2:260-263.
2. Jespers A, Buntinx I, Melis K, Vaerenberg M, Janssens G (1993): Two siblings with midline field defects and Hirschsprung disease: Variable expression of Toriello-Carey or new syndrome? Am J Med Genet 47:299-302.
3. Lacombe D, Creusot G, Battin J (1992): New case of Toriello-Carey syndrome. Am J Med Genet 42:374-376.
4. Toriello HV, Carey JC (1988): Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: A new autosomal recessive syndrome? Am J Med Genet 31:17-23.