Poland Syndrome- A Rare Congenital Condition

Authors

  • Homayra Tahseen Hossain Associate Professor, Medicine, Popular Medical College Hospital, Dhaka
  • Md Abul Kashem Khandaker Professor & Head of Medicine, Popular Medical College Hospital, Dhaka
  • Quazi Tarikul Islam Professor of Medicine, Popular Medical College Hospital, Dhaka
  • HAM Nazmul Ahasan Professor of Medicine, Popular Medical College Hospital, Dhaka
  • Munshi MB Md Shoaib Adnan Registrar, Medicine, Popular Medical College Hospital, Dhaka
  • Nazmul Islam Intern Doctor, Popular Medical College Hospital, Dhaka

DOI:

https://doi.org/10.3329/jbcps.v36i4.38186

Keywords:

Poland Syndrome, symbrachydactyly

Abstract

Named after Sir Alfred Poland, Poland syndrome is a rare congenital anomaly classically characterized by the absence of unilateral chest wall muscles and sometimes ipsilateral symbrachydactyly (abnormally short and webbed fingers). The aetiology is probably a vascular disruption sequence of the subclavian arteries. In most cases, Poland Syndrome is sporadic. We report a 26 year old male patient with typical features of Poland Syndrome associated with bronchiectasis and mitral valve prolapse- a very rare association. To the best of our knowledge, this is the first documented case of a Poland Syndrome with rare association reported from Bangladesh.

J Bangladesh Coll Phys Surg 2018; 36(4): 166-169

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Published

2018-09-14

How to Cite

Hossain, H. T., Khandaker, M. A. K., Islam, Q. T., Ahasan, H. N., Adnan, M. M. M. S., & Islam, N. (2018). Poland Syndrome- A Rare Congenital Condition. Journal of Bangladesh College of Physicians and Surgeons, 36(4), 166–169. https://doi.org/10.3329/jbcps.v36i4.38186

Issue

Vol. 36 No. 4 (2018)

Section

Case Reports

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