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A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.

Anna ZlotinaOlesia MelnikYulia FomichevaRostislav SkitchenkoAlexey SergushichevElena ShagimardanovaOleg GusevGuzel GazizovaTatiana LoevetsTatiana VershininaIvan KozyrevMikhail GordeevElena VasichkinaTatiana PervuninaAnna Kostareva
Published in: BMC medical genomics (2020)
The results support the previous data, indicating that complete ZRS duplication underlies TPT-PS, and suggest a broader phenotypic impact of the 7q36.3 microduplication. Potential involvement of the 7q36.3 microduplication in the patient's cardiac and eye malformations is discussed. However, the contribution of some additional genetic/epigenetic factors to the complex patient`s phenotype cannot be excluded entirely. Further comprehensive functional studies are needed to prove the possible involvement of the 7q36.3 locus in congenital heart disease and eye pathology.
Keyphrases
  • case report
  • congenital heart disease
  • gene expression
  • left ventricular
  • machine learning
  • genome wide
  • optical coherence tomography
  • risk assessment
  • atrial fibrillation
  • copy number
  • human health