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Mosaic ring chromosome 6 in an infant with significant patent ductus arteriosus and multiple congenital anomalies. | LitMetric

AI Article Synopsis

  • The clinical symptoms of ring chromosome 6 include issues with the central nervous system, growth delays, distinct facial features, and other birth defects.
  • A case is presented involving a 7-day-old male infant who had mosaic ring chromosome 6, a significant patent ductus arteriosus (PDA), and underdeveloped heart structures, which are unusual associations with this condition.
  • After surgery to close the PDA, the infant improved but continued to face challenges such as failure to thrive and delayed developmental milestones during follow-up, marking it as the first documented case of a Korean individual with this chromosomal abnormality and significant PDA.

Article Abstract

The clinical features of ring chromosome 6 include central nervous system anomalies, growth retardation, facial dysmorphism and other congenital anomalies. Ring chromosome 6 occurs rarely and manifests as various phenotypes. We report the case of mosaic ring chromosome 6 by conventional karyotyping in a 7-day-old male infant diagnosed with a large patent ductus arteriosus (PDA) with hypoplasia of aortic valve and aortic arch. These have not been previously reported with ring chromosome 6. He recovered from heart failure symptoms after ligation of the PDA. He showed infantile failure to thrive and delayed milestone in a follow-up evaluation. To the best of our knowledge, this is the first report of a Korean individual with ring chromosome 6 and hemodynamically significant PDA.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410245PMC
http://dx.doi.org/10.3346/jkms.2012.27.8.948DOI Listing

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