Thrombocytopenia in Newborn with Holt-Oram Syndrome: A Rare Case Report

Authors

  • Manish Sah Manipal College of Medical Sciences
  • Raj Kumar Shah Manipal College of Medical Sciences
  • Eva Gauchan Manipal College of Medical Sciences

Keywords:

Heart-hand Syndrome, Holt-Oram Syndrome, Newborn

Abstract

Holt-Oram syndrome or heart-hand syndrome is a rare congenital disorder characterized by a combination of upper limb abnormalities and congenital heart lesions. We report a case of a neonate with congenital anomalies of the left upper limb (radial club hand, absent radius bone, and absent thumb) with multiple cardiac defects (atrial septal defect, ventricular septal defect, and patent ductus arteriosus). This case report emphasizes the need for screening of cardiac anomalies in all newborns with upper limb deformities.

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Author Biographies

Manish Sah, Manipal College of Medical Sciences

Department of Paediatrics, Resident

Raj Kumar Shah, Manipal College of Medical Sciences

Department of Pediatrics, Resident

Eva Gauchan, Manipal College of Medical Sciences

Department of Pediatrics, Professor

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Published

2024-12-27

How to Cite

Sah, M., Shah, R. K., & Gauchan, E. (2024). Thrombocytopenia in Newborn with Holt-Oram Syndrome: A Rare Case Report . Nepal Journal of Medical Sciences, 9(2). Retrieved from https://nepjol.info/index.php/NJMS/article/view/72348

Issue

Section

Case Reports