Congenital emphysema, cryptorchidism, penoscrotal web, deafness, and mental retardation - A new syndrome?

Clinical Dysmorphology

Volumn 6, Issue 1, 1997, Pages 35-37

  Lynch, S A ^a   Bushby, K M D ^a  

^a Department of Human Genetics ^*  (United Kingdom)

Author keywords

congenital emphysema; constipation; cryptorchidism; deafness; penoscrotal web

Indexed keywords

ARTICLE; CASE REPORT; CRYPTORCHISM; EMPHYSEMA; GENITAL MALFORMATION; HEARING IMPAIRMENT; HUMAN; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL; SCHOOL CHILD; SYNDROME DELINEATION;

EID: 0031027128     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199701000-00006     Document Type: Article

References (6)

1. Edwards JA, Sethi PK, Scoma AJ et al. (1976): A new familial syndrome characterised by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance. Am J Med 60: 23-32.
2. Goldstein JL, Fialkow PJ (1973): The Alstrom syndrome. Report of three cases with further delination of the clinical, pathophysiological and genetic aspects of the disorder. Medicine 52: 53-71.
3. Sanderson DM, Fraser FC (1983): Case report 99. J Clin Dysmorphol 1: 19-21.
4. Thompson E, Baraitser M (1987): Syndrome of the month: FG syndrome. J Med Genet 24: 139-143.
5. Winter RM, Baraitser M (1992): "London Dysmorphology Database". Oxford: Oxford University Press.
6. Yolken R, Konecny P, Effman EL (1976): Case report 48. Synd Ident 4: 13-16.