A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature | BMC Medical Genomics | Full Text

A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature | BMC Medical Genomics | Full Text

A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature

Proximal microdeletions on chromosome 15q25.2 are very rare, and are associated with neurodevelopmental delay, inguinal hernia, chest deformities, and anemia. The minimum length missed so far is 1.4 Mb. Howeve...

Authors:Zhen Chen, Hong Chen, Ke Yuan and Chunlin Wang

Citation:BMC Medical Genomics 2020 13:126

Content type:Case report

 

Published on: 7 September 2020

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