Noonan Syndrome with Hepatomegaly and Persistently Elevated Liver Enzymes: A Case Report

Authors

  • Md Aminul Islam Junior Consultant (Medicine), Upazilla Health Complex, Charghat, Rajshahi, Bangladesh
  • Shamrose Begum Lecturer, Anatomy, Rajshahi Medical College, Rajshahi, Bangladesh
  • Md Azizul Haque Associate Professor, Medicine, Rajshahi Medical College, Rajshahi, Bangladesh

DOI:

https://doi.org/10.3329/taj.v35i1.61168

Keywords:

Noonan Syndrome, liver enzymes

Abstract

Noonan’s syndrome is a polymorphic disorder with some facial features, congenital heart defects, cryptorchidism, etc., and also associated with some autoimmune diseases, lymphatic dysplasias. Here we are reporting a nine years old boy with Noonan's syndrome who has hepatomegaly with persistently raised hepatic enzymes, which remained unexplained.

TAJ 2022; 35: No-1: 137-140

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Published

2022-08-10

How to Cite

Islam, M. A. ., Begum, S. ., & Haque, M. A. . (2022). Noonan Syndrome with Hepatomegaly and Persistently Elevated Liver Enzymes: A Case Report. TAJ: Journal of Teachers Association, 35(1), 137–140. https://doi.org/10.3329/taj.v35i1.61168

Issue

Vol. 35 No. 1 (2022)

Section

Case Reports