Bardet Biedl Syndrome- A Case Report

Authors

  • M Azizul Haque Resident Physician, Department of Medicine, Rajshahi Medical College & Hospital, Rajshahi.
  • LS Sharmin Post graduate Student, FCPS (Pediatrics) Part 2 , BSMMU, Dhaka.
  • Q Tarikul Islam Professor and Head, Department of Medicine, Rajshahi Medical College, Rajshahi.
  • ARM Saifuddin Ekram Professor, Department of Medicine, Rajshahi Medical College, Rajshahi.

DOI:

https://doi.org/10.3329/taj.v20i1.3092

Abstract

Bardet Biedl syndrome is a rare autosomal recessive condition with a wide spectrum of clinical features. The accepted major criteria for diagnosis include retinal dystrophy, obesity, polydactyly, male hypogonadism, mental retardation and renal dysfunction. We have presented a 16 year old male patient exhibiting characteristic features of Bardet Biedl syndrome (BBS) and then the literature is reviewed.  

doi: 10.3329/taj.v20i1.3092

TAJ 2007; 20(1):56-59

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How to Cite

Haque, M. A., Sharmin, L., Islam, Q. T., & Ekram, A. S. (2009). Bardet Biedl Syndrome- A Case Report. TAJ: Journal of Teachers Association, 20(1), 56–59. https://doi.org/10.3329/taj.v20i1.3092

Issue

Vol. 20 No. 1 (2007)

Section

Case Reports