Name: PubCaseFinder
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).

Microcephaly

Head circumference below 2 standard deviations below the mean for age and gender.

Total: 1

(per page)

PMID (PMCID)
23056899 (3446055)	OTHER
	Triple x syndrome with short stature: case report and literature review.
	Li M, Zou C, Zhao Z. Iran J Pediatr. 2012;22(2):269-73.
	Triple X syndrome is a sex chromosomal aneuploidy condition characterized by tall stature, microcephaly, hypertelorism, congenital abnormalities, and motor and language delays.