Noonan’s Syndrome of a 25 years old female

Authors

  • M Sirajul Haque Prof and Head of the Department of Dermatology and Venereal Disease, Bangladesh Medical College
  • Riaz Uddin Ahmed Assistant Prof of Department of Dermatology and Venereal disease, Bangladesh Medical College
  • Md Mahmudur Rahman Lecturer, Department of Pharmacology, Ibn Sina Medical College

DOI:

https://doi.org/10.3329/bjms.v8i3.3986

Keywords:

Noonan's syndrome, genetic disorders

Abstract

Noonan's syndrome is an autosomal dominant disorder with a webbed neck that mimics turner syndrome. However, the syndrome has also been found to be genetically heterogeneous. Noonan syndrome is characterized by short stature, hyperkeratosis of skin, distinct facial features, lymphoreticular abnormalities, nail dystrophy. No abnormality in chromosome number has so far been reported. Here we present a 25 year old female who came to Bangladesh Medical College Hospital in May'08, with generalized skin eruptions and left leg swelling.

Key words: Noonan's syndrome, genetic disorders

DOI: 10.3329/bjms.v8i3.3986

Bangladesh Journal of Medical Sciences Vol.8(3) 2009 p68-71

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How to Cite

Haque, M. S., Ahmed, R. U., & Rahman, M. M. (2009). Noonan’s Syndrome of a 25 years old female. Bangladesh Journal of Medical Science, 8(3), 68–71. https://doi.org/10.3329/bjms.v8i3.3986

Issue

Section

Case Reports