Literature DB >> 33731094

One healthy live birth after preimplantation genetic testing of a cryptic balanced translocation (9;13) in a family with cerebral palsy and glaucoma: a case report.

Xiliang Wang1, Changsheng Wu2, Dongmei Hao1, Jinyan Zhang1, Chang Tan1, De-Hua Cheng3, Jia Fei4, Yuexin Yu5.   

Abstract

BACKGROUND: Cryptic balanced translocations often evade detection by conventional cytogenetics. The preimplantation genetic testing (PGT) technique can be used to help carriers of balanced translocations give birth to healthy offspring; however, for carriers of cryptic balanced translocations, there is only one report about trying assisted reproduction using the PGT technique but with no pregnancy. CASE
PRESENTATION: A couple had 3 births out of 4 pregnancies, and all died very young, with two of them having both cerebral palsy and glaucoma. The husband with oligoasthenospermia was found to be a cryptic balanced translocation carrier for t (9,13) (p24.3, q31.3) with G-banding, FISH (fluorescence in-situ hybridization), and MicroSeq techniques; live birth of a healthy baby girl was achieved with PGT/NGS (next-generation sequencing) for the couple.
CONCLUSION: Here, we report for the first time a successful live birth of a healthy baby through the PGT technique for a family in which the husband is a carrier of the cryptic balanced translocation t (9,13) (p24.3, q31.3), presumably causative for cerebral palsy and glaucoma. Our study showed that the PGT/NGS technique can effectively help families with a cryptic balanced translocation have healthy offspring.

Entities:  

Keywords:  Cryptic balanced translocation; FISH; G-banding; Preimplantation genetic testing

Year:  2021        PMID: 33731094      PMCID: PMC7972244          DOI: 10.1186/s12920-021-00938-7

Source DB:  PubMed          Journal:  BMC Med Genomics        ISSN: 1755-8794            Impact factor:   3.063


  18 in total

Review 1.  Preimplantation genetic diagnosis of structural abnormalities.

Authors:  S Munné
Journal:  Mol Cell Endocrinol       Date:  2001-10-22       Impact factor: 4.102

2.  Preimplantation genetic diagnosis for a known cryptic translocation: follow-up clinical report and implication of segregation products.

Authors:  L J McKenzie; P L Cisneros; S Torsky; C A Bacino; J E Buster; S A Carson; J L Simpson; F Bischoff
Journal:  Am J Med Genet A       Date:  2003-08-15       Impact factor: 2.802

3.  Evaluation of preimplantation genetic testing based on next-generation sequencing for balanced reciprocal translocation carriers.

Authors:  Yunni Cai; Min Ding; Fei Lin; Zhenyu Diao; Ningyuan Zhang; Haixiang Sun; Jianjun Zhou
Journal:  Reprod Biomed Online       Date:  2019-01-08       Impact factor: 3.828

4.  A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration.

Authors: 
Journal:  Nat Genet       Date:  1996-09       Impact factor: 38.330

Review 5.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

6.  Clinical and genetic characterization of a patient with SOX5 haploinsufficiency caused by a de novo balanced reciprocal translocation.

Authors:  Daisuke Fukushi; Kenichiro Yamada; Kaoru Suzuki; Mie Inaba; Noriko Nomura; Yasuyo Suzuki; Kimiko Katoh; Seiji Mizuno; Nobuaki Wakamatsu
Journal:  Gene       Date:  2018-03-22       Impact factor: 3.688

7.  Pregnancy outcomes of reciprocal translocation carriers with two or more unfavorable pregnancy histories: before and after preimplantation genetic testing.

Authors:  Caiyi Huang; Wenjie Jiang; Yueting Zhu; Hongchang Li; Juanjuan Lu; Junhao Yan; Zi-Jiang Chen
Journal:  J Assist Reprod Genet       Date:  2019-09-14       Impact factor: 3.412

8.  Predictive value of sperm fluorescence in situ hybridization analysis on the outcome of preimplantation genetic diagnosis for translocations.

Authors:  Tomas Escudero; Iman Abdelhadi; Mireia Sandalinas; Santiago Munné
Journal:  Fertil Steril       Date:  2003-06       Impact factor: 7.329

9.  Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGH.

Authors:  Eleonora Di Gregorio; Elisa Savin; Elisa Biamino; Elga Fabia Belligni; Valeria Giorgia Naretto; Gaetana D'Alessandro; Giorgia Gai; Franco Fiocchi; Alessandro Calcia; Cecilia Mancini; Elisa Giorgio; Simona Cavalieri; Flavia Talarico; Patrizia Pappi; Marina Gandione; Monica Grosso; Valentina Asnaghi; Gabriella Restagno; Giorgia Mandrile; Giovanni Botta; Margherita Cirillo Silengo; Enrico Grosso; Giovanni Battista Ferrero; Alfredo Brusco
Journal:  Mol Cytogenet       Date:  2014-11-19       Impact factor: 2.009

Review 10.  Fluorescence In situ Hybridization: Cell-Based Genetic Diagnostic and Research Applications.

Authors:  Chenghua Cui; Wei Shu; Peining Li
Journal:  Front Cell Dev Biol       Date:  2016-09-05
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