Apert Syndrome

Authors

  • KG Mostafa Assistant Professor of Paediatrics, Khulna Medical College, Khulna
  • CH Rasul Professor of Paediatrics, Khulna Medical College, Khulna
  • NN Baruri Assistant Professor of Paediatrics, Khulna Medical College, Khulna
  • SM Rahman Assistant Registrar of Paediatrics, Khulna Medical College Hospital, Khulna

DOI:

https://doi.org/10.3329/bmjk.v44i1-2.10473

Keywords:

Apert Syndrome

Abstract

Apert syndrome is a rare autosomal dominant malformation. In the recent past we encountered a boy of 16 months with fusion of both fingers and toes, dysmorphic facial features presenting with cough and respiratory distress in Khulna Medical College hospital. Considering the general paucity of cases of acrocephalosyndactyly in the Bangladeshi literature, this case demands reporting. Careful evaluation is necessary in a doubtful case to optimize the treatment.

DOI: http://dx.doi.org/10.3329/bmjk.v44i1-2.10473

Bang Med J (Khulna) 2011: 44(1&2) 25-27

Downloads

Download data is not yet available.
Abstract
154
PDF
242

Downloads

Published

2012-04-23

How to Cite

Mostafa, K., Rasul, C., Baruri, N., & Rahman, S. (2012). Apert Syndrome. Bangladesh Medical Journal Khulna, 44(1-2), 25–27. https://doi.org/10.3329/bmjk.v44i1-2.10473

Issue

Vol. 44 No. 1-2 (2011)

Section

Case Reports

License

Copyright is normally held by the author of the article.