Brief Clinical Report: Toriello-Carey syndrome: Case report with additional findings

American Journal of Medical Genetics

Volumn 98, Issue 3, 2001, Pages 273-276

  Aftimos, S ^a,b   McGaughran, J ^a  

^a Northern Regional Genetics Service   (New Zealand)

^b AUCKLAND CITY HOSPITAL   (New Zealand)

Author keywords

Agenesis of the corpus callosum; Anal anomalies; Blepharophimosis; DiGeorge VCF syndrome; Opitz BBBG syndrome; Pierre Robin sequence; Toriello Carey syndrome

Indexed keywords

ANORECTAL MALFORMATION; ARTICLE; BLEPHAROPHIMOSIS; CASE REPORT; CONGENITAL HEART DISEASE; CORPUS CALLOSUM AGENESIS; DEVELOPMENTAL DISORDER; DIGEORGE SYNDROME; EAR MALFORMATION; FEMALE; HUMAN; INFANT; MALE; MULTIPLE MALFORMATION SYNDROME; PIERRE ROBIN SYNDROME; PRIORITY JOURNAL; SEX DIFFERENCE; SYNDROME DELINEATION; TELECANTHUS; TORIELLO CAREY SYNDROME; X CHROMOSOME LINKAGE; ANAL CANAL; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; CORPUS CALLOSUM; FATALITY; FOOT MALFORMATION; NEWBORN; PATHOLOGY; SYNDROME;

ERETMOCHELYS IMBRICATA;

ABNORMALITIES, MULTIPLE; ANAL CANAL; BLEPHAROPHIMOSIS; CORPUS CALLOSUM; FATAL OUTCOME; FEMALE; FOOT DEFORMITIES, CONGENITAL; HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; SYNDROME;

EID: 0035931508     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010122)98:3<273::AID-AJMG1081>3.0.CO;2-4     Document Type: Article

References (10)

1. Toriello-Carey syndrome: Report of a new case
2. Two sisters with the Toriello-Carey syndrome
3. Toriello-Carey syndrome: Evidence for X-linked inheritance
4. Two siblings with midline field defects and Hirschprung disease: Variable expression of Toriello-Carey or new syndrome?
5. New case of Toriello-Carey syndrome
6. Toriello-Carey syndrome with endocardial fibroelastosis
7. G syndrome (Hypertelorism with esophageal abnormality and hypospadias, or hypospadias-dysphagia, or "Opitz-Frias" or "Opitz G" syndrome) - Perspective in 1987 and bibliography
8. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study
9. Toriello-Carey syndrome
10. Corpus callosum agenesis, facial anomalies. Robin sequence, and other anomalies: A new autosomal recessive syndrome?