What syndrome is this?

Pediatric Dermatology

Volumn 13, Issue 6, 1996, Pages 507-508

  Llistosella, Enric ^a   Pujol, Ramon M ^b  

^a HOSPITAL JOSEP TRUETA   (Spain)

^b Sant Pau University Hospital   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; HUMAN; KIDNEY AGENESIS; MALE; MALFORMATION SYNDROME; PERCEPTION DEAFNESS; PRESCHOOL CHILD; PRIORITY JOURNAL; SKIN NODULE; SYNDROME DELINEATION; BRANCHIOOTORENAL SYNDROME; CONGENITAL MALFORMATION; FATHER; KIDNEY;

BRANCHIO-OTO-RENAL SYNDROME; CHILD, PRESCHOOL; FATHERS; HEARING LOSS, SENSORINEURAL; HUMANS; KIDNEY; MALE;

EID: 0030463203     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1525-1470.1996.tb00735.x     Document Type: Article

References (5)

1. Menick M, Bixler D, Nance WE, et al. Familial branchio-oto-renal dysplasia: a new addition to the branchial arch syndromes. Clin Genet 1976;9:23-34.
2. Fraser FC, Ling D, Clogg D, et al. Genetic aspects of the BOR syndrome - branchial fistulas, ears pits, hearing loss, and senal anomalies. Am J Med Genet 1978;2:241-252.
3. Heimler A, Lieber E. Branchio-Oto-Renal Syndrome: Reduced penetrance and variable expressivity in four generations of a large kindred. Am J Med Genet 1986;25:15-27.
4. Lachiewicz AM, Sibley R, Michael AF. Hereditary renal disease and preauricular pits: Report of a kindred. J Pediatr 1985;106:948-950.
5. Torres-Peris V, Jorda E, Ramon D, et al. Melnick-Fraser Syndrome. Dermatology 1994;189:103-104.