Print ISSN:-2394-2746

Online ISSN:-2394-2754

CODEN : IJOGCS

Current Issue

Year 2019

Volume: 6 , Issue: 4

Article view: 270

Article download: 151

Indian Journal of Obstetrics and Gynecology Research


A case report of infant with robertsonian translocation


Full Text PDF Share on Facebook Share on Twitter


Author Details : Darshna Pandya, Manish Pandya*, Shrina Shah, Jiten Senta

Volume : 6, Issue : 1, Year : 2019

Article Page : 119-121


Suggest article by email


Abstract

Robertsonian translocations carry reproductive risks that are dependent on the chromosomes involved and the sex of the carrier Robertsonian translocation (14:15)(q10;q10)4p is rare and account for only 0.6%.
We describe a case with rob (14;15) in which the phenotype includes:
Generalized hypotonia, respiratory distress, high arch palate, left ear-grooves abnormal, prominent nasal bridge, left impatent nasolacrimal duct, dysmorphic face.
Chromosome analysis with peripheral blood was performed, while the karyotype was interpreted as 45,XX, der (14;15)(q10;q10)4p.out of two chromosome number 4, one Chromosome 4 has found deleted from 'p' arm small arm In wolf-hirschhorn Syndrome.
Molecular studies associated with spinal muscular atrophy and progressive muscular dystrophy also had negative findings. We suggest that rob(14;15)(q10;q10)4p could be Related to clinical presentation like this case.

Keywords: PGD, reproductive risks, Robertsonian translocation, Chromosomes, Down syndrome, Aneuploidy, Trisomy, Translocation (genetics), Mosaicism, Preimplantation diagnosis.

Doi : 10.18231/2394-2754.2019.0029

How to cite : Pandya D, Pandya M, Shah S, Senta J, A case report of infant with robertsonian translocation. Indian J Obstet Gynecol Res 2019;6(1):119-121

Copyright © 2019 by author(s) and Indian J Obstet Gynecol Res. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (creativecommons.org)