<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang X</submitter><funding>Family Planning Research Fund</funding><pagination>82</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7972244</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>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.&lt;h4>Case presentation&lt;/h4>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.&lt;h4>Conclusion&lt;/h4>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.</pubmed_abstract><journal>BMC medical genomics</journal><pubmed_title>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.</pubmed_title><pmcid>PMC7972244</pmcid><funding_grant_id>19JSZ12</funding_grant_id><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Cheng DH</pubmed_authors><pubmed_authors>Wu C</pubmed_authors><pubmed_authors>Tan C</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Fei J</pubmed_authors><pubmed_authors>Hao D</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>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.</name><description>&lt;h4>Background&lt;/h4>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.&lt;h4>Case presentation&lt;/h4>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.&lt;h4>Conclusion&lt;/h4>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.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-25T19:31:08.32Z</modification><creation>2025-04-06T07:58:16.273Z</creation></dates><accession>S-EPMC7972244</accession><cross_references><pubmed>33731094</pubmed><doi>10.1186/s12920-021-00938-7</doi></cross_references></HashMap>