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 Department of Paediatrics & Neonatology, Karnali Academy of Health Sciences, Jumla Karnali
  • Annie Shrestha Department of Paediatrics & Neonatology, Karnali Academy of Health Sciences, Jumla Karnali

Keywords:

Cryptophthalmos, Fraser Syndrome, Neonate, Syndactyly

Abstract

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

Downloads

Download data is not yet available.
Abstract
3
PDF
0

Downloads

Published

2022-12-30

How to Cite

Shrestha, S., Thani, K. P., Keshari, M., & Shrestha, A. (2022). Fraser Syndrome: A Rare Case Report. Journal of Karnali Academy of Health Sciences, 5(3). Retrieved from https://nepjol.info/index.php/jkahs/article/view/86573

Issue

Vol. 5 No. 3 (2022)

Section

Case Reports

License

Copyright (c) 2022 Sandeep Shrestha, Kamal Prasad Thani, Munna Keshari, Annie Shrestha

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.