Goeminne syndrome (omim 314300): Another male patient 30 years later

Genetic Counseling

Volumn 14, Issue 1, 2003, Pages 109-111

  Fryns, J P ^a,b   Gevers, D ^c  

^a University Hospital Gasthuisberg   (Belgium)

^b CENTER FOR HUMAN GENETICS   (Belgium)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; AUTOSOME; CASE REPORT; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION; CHROMOSOME XQ; CLINICAL FEATURE; CRYPTORCHISM; GENE LOCATION; GOEMINNE SYNDROME; HUMAN; KELOID; KIDNEY DYSPLASIA; MALE; TORTICOLLIS; X CHROMOSOME LINKED DISORDER;

ABNORMALITIES, MULTIPLE; ADULT; CERVICAL VERTEBRAE; CHROMOSOMES, HUMAN, X; CRYPTORCHIDISM; FOLLOW-UP STUDIES; GENES, DOMINANT; HUMANS; KELOID; KIDNEY; KYPHOSIS; LINKAGE (GENETICS); MALE; SCOLIOSIS; SEX CHROMOSOME ABERRATIONS; SYNDROME; THORACIC VERTEBRAE; TORTICOLLIS;

EID: 0037245056     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (2)

1. GOEMINNE L.: A new probably X-linked inherited syndrome (congenital muscular torticollis, multiple keloids, cryptorchidism and renal dysplasia. Acta Genet. Med. Gemellol., 1968, 17, 439-467.
2. ZUFFARDI O., FRACCARO M.: Gene Mapping and Serendipity. The Locus for Torticollis, Keloids, Cryptorchidism and Renal Dysplasia (31430 McKusick) is at Xq28, Distal to the G6PD Locus. Hum. Genet., 1982, 62, 280-281.