Branchio-oculo-facial syndrome associated with a white forelock

Clinical Dysmorphology

Volumn 7, Issue 3, 1998, Pages 221-223

  Megarbane A ^a,d   Hawat, N ^b   Chedid, P ^b   Bleik, J ^b   Delezoide Al ^c  

^a SAINT JOSEPH UNIVERSITY   (Lebanon)

^b RIZK HOSPITAL   (Lebanon)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d Saint Joseph University   (France)

Author keywords

Branchio oculo facial syndrome; White forelock

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRANCHIAL DEFECT; CASE REPORT; DISEASE ASSOCIATION; EXON; FACE MALFORMATION; FEMALE; GENETIC ANALYSIS; HUMAN; INFANT; MALE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADULT; BRANCHIAL REGION; EYE ABNORMALITIES; FACIES; FEMALE; HAIR COLOR; HUMANS; MALE; SYNDROME;

EID: 0031868706     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199807000-00013     Document Type: Article

References (4)

1. Abdelhak S, Kalatzis V, Heilig R, Compain S, Samson D, Vincent C, Weil D, Cruaud C, Sahly I, Leibovici M, Bitner-Glindzicz M, Francis M, Lacombe D, Vigneron J, Charachon R, Boven K, Bedbeder P, Van Regemorter N, Weissenbach J, Petit C (1997). A human homologue of the Drosophilia eyes absent gene underlies Branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Nature Genet 15;2:157-164.
2. Legius E, Fryns JP, Van Den Berghe H (1990). Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndrome. Clin Genet 37:347-350.
3. Lin AE, Gorlin RJ, Lurie IW, Brunner H, van der Burgt I, Naumchik I, Rumyantseva N, Stengel-Rutkowski S, Rosenbaum K, Meinecke P, Muller D (1995). Further delineation of the branchio-oculo-facial syndrome. Am J Med Genet 56:42-59.
4. Rizzo R, Micali G, Calvieri S, Sorge G, Mazzone D (1995). Branchio-oculo-facial syndrome and dermal thymus: case report and review of the literature. Pediatr Dermatol 12:24-27.