Fraser Syndrome: A Rare Case Report

Authors

  • Sandeep Shrestha Department of Paediatrics & Neonatology, Karnali Academy of Health Sciences, Jumla, Karnali
  • Kamal Prasad Thani Department of Paediatrics & Neonatology, Karnali Academy of Health Sciences, Jumla, Karnali
  • Munna Keshari Resident, Department of Paediatrics & Neonatology, Karnali Academy of Health Sciences, Jumla, Karnali
  • Annie Shrestha Nursing Officer, Department of Paediatrics & Neonatology, Karnali Academy of Health Sciences, Jumla, Karnali

DOI:

https://doi.org/10.61814/jkahs.v5i3.753

Keywords:

Cryptophthalmos, Fraser Syndrome, Neonate, Syndactyly

Abstract

Fraser syndrome is a rare, autosomal recessive condition. It is characterized by cryptophthalmos, syndactyly, craniofacial dysmorphism, laryngeal and genitourinary malformations, and musculoskeletal anomalies. We report a case of a neonate who presented with multiple congenital abnormalities and clinical features suggestive of Fraser syndrome.

Published

2022-12-31

How to Cite

1.
Shrestha S, Thani KP, Keshari M, Shrestha A. Fraser Syndrome: A Rare Case Report. Journal of Karnali Academy of Health Sciences [Internet]. 2022Dec.31 [cited 2024Apr.27];5(3). Available from: https://jkahs.org.np/jkahs/index.php/jkahs/article/view/753

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