Genetic and phenotypic continuum of HOXA genes: A case with double HOXA9/HOXA13 mutations.

ABSTRACT: The HOXA genes cluster plays a key role in embryologic development. Mutations in HOXA genes have been linked to different human phenotypes, including developmental delay, limb anomalies, and urogenital malformations. The present study reported a clinical and genetic investigation of a female patient with polymalformative syndrome including left arm agenesis, bicornuate uterus and bicuspid aortic valve. Using whole exome sequencing, two heterozygous missense variants were identified. Of these, one was a novel variant in the HOXA13 gene [p.(Tyr290Ser)] and the second a heterozygous variant in the HOXA9 gene [p.(Ala102Pro)]. To the best of our knowledge, this is the first association of HOXA9/HOXA13 point mutations linked to a syndromic case. In conclusion,

SUBMITTER: Jaouadi H 

PROVIDER: S-EPMC9936258 | biostudies-literature | 2023 Mar

REPOSITORIES: biostudies-literature