Please use this identifier to cite or link to this item:
|Title:||Triple X syndrome with rare phenotypic presentation.|
|Citation:||Jagadeesh S, Jabeen G, Bhat L, Vasikarla M, Suresh A, Seshadri S, Lata S. Triple X syndrome with rare phenotypic presentation. Indian Journal of Pediatrics. 2008 Jun; 75(6): 629-31|
|Abstract:||Triple X syndrome is a rare numerical chromosomal anomaly, occurring as a result of non dysjunction in meiosis I. Most cases have neurodevelopmental defects and functional problems. We report two cases diagnosed in our centre. The first was a fetus with cleft lip and palate, 47, XXX was identified by Fetal Blood Sampling. The second was a child with multisystem anomaly including cleft lip and palate, whose karyotype also revealed 47, XXX. Though isolated cases of associated abnormalities have been reported there have not been consistent phenotypic changes reported with this condition.|
|Appears in Collections:||Indian Journal of Pediatrics|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.