Dental findings of a child with Wolf-Hirschhorn syndrome

International Journal of Paediatric Dentistry

Volumn 16, Issue 2, 2006, Pages 139-142

  Johnston, N J ^a   Franklin, D L ^a  

^a BRISTOL DENTAL HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 4; CHROMOSOME DELETION; CONGENITAL MALFORMATION; CRANIOFACIAL MALFORMATION; DECIDUOUS TOOTH; FACIES; FEMALE; HEART SEPTUM DEFECT; HUMAN; HYPODONTIA; LEARNING DISORDER; MOLAR TOOTH; MULTIPLE MALFORMATION SYNDROME; SYNDROME; TOOTH CROWN;

ABNORMALITIES, MULTIPLE; ANODONTIA; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; CRANIOFACIAL ABNORMALITIES; FACIES; FEMALE; HEART SEPTAL DEFECTS, ATRIAL; HUMANS; LEARNING DISORDERS; MOLAR; SYNDROME; TOOTH CROWN; TOOTH, DECIDUOUS;

EID: 33645129815     PISSN: 09607439     EISSN: 1365263X     Source Type: Journal    
DOI: 10.1111/j.1365-263X.2006.00675.x     Document Type: Article

References (8)

1. Wolf U Reinwein H Porsch R Schroter R Baitsch H. [Deficiency on the short arms of a chromosome No. 4]. Humangenetik 1965 1 397 413.
2. Hirschhorn K Cooper HL Firschein IL. Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion. Humangenetik 1965 1 479 482.
3. Wilson M Towner J Negus L. Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4. Journal of Medical Genetics 1970 7 164 170.
4. Battalgia A Carey J Wright T. Wolf-Hirschhorn (4p-) syndrome. Advances in Paediatrics 2001 48 75 113.
5. Breen GH. Taurodontism, an unreported dental finding in Wolf-Hirschhorn (4p) syndrome. Journal of Dentistry for Children. 1998 65 344 345 356.
6. Burgersdijk R Tan HL. Oral symptoms of the Wolf syndrome: report of a case. Journal of Dentistry for Children 1978 45 488 489.
7. Nieminen P Kotilainen J Aalto Y Knuutila S Pirinen S Thesleff I. MSX1 Gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia. Journal of Dental Research 2003 82 1013 1017.
8. Kozma C Chong S Meck J. Interstitial deletion of 4p15· 32p16·3 in a boy with minor anomalies, hearing loss, borderline intelligence, and oligodontia. American Journal of Medical Genetics 1999 8 86 316 320.