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License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Trisomy X

Trisomy X is a sex chromosome anomaly with a variable phenotype caused by the presence of an extra X chromosome in females (47,XXX instead of 46,XX).

Radioulnar synostosis

An abnormal osseous union (fusion) between the radius and the ulna.

Total: 1

(per page)

PMID (PMCID)
7281903	MIXED_SAMPLE	Child
	[Radioulnar synostosis as characteristic feature of chromosome aberrations (author's transl)].
	Kusswetter W, Heisel A. Z Orthop Ihre Grenzgeb. 1981;119(1):10-3.
	Among 13 patients with congenital proximal radioulnar synostosis the chromosomal analysis revealed a 47, XXY-constellation in an 8 years old boy and a 47, XXX-syndrome in a 12-year-old girl.