Association of Haemophilia with Down Syndrome

Authors

  • Gursharan Singh Narang Department of Paediatrics, Sri Guru Ram Das Institute of Medical Sciences and Research, Vallah, Amritsar
  • Tarsem Singh Department of Paediatrics, Sri Guru Ram Das Institute of Medical Sciences and Research, Vallah, Amritsar
  • Anubha Sharma Department of Paediatrics, Sri Guru Ram Das Institute of Medical Sciences and Research, Vallah, Amritsar
  • Supriya Malik Department of Paediatrics, Sri Guru Ram Das Institute of Medical Sciences and Research, Vallah, Amritsar
  • Amandeep Kaur Resident, Department of Paediatrics, Sri Guru Ram Das Institute of Medical Sciences and Research, Vallah, Amritsar

DOI:

https://doi.org/10.3126/jnps.v36i1.11949

Keywords:

Hemophilia B, Down’s syndrome

Abstract

Hemophilia B is a hereditary bleeding disorder caused by a lack of blood clotting factor IX. Without enough factor IX, the blood cannot clot properly to control bleeding. Hemophilia B presenting in association with Down’s syndrome is quite rare. We report a case of a one month old child who presented to us with continuous unexplained bleeding.

J Nepal Paediatr Soc 2016;36(1):75-77.

Downloads

Download data is not yet available.
Abstract
1271
PDF
837

Author Biographies

Gursharan Singh Narang, Department of Paediatrics, Sri Guru Ram Das Institute of Medical Sciences and Research, Vallah, Amritsar

Professor

Tarsem Singh, Department of Paediatrics, Sri Guru Ram Das Institute of Medical Sciences and Research, Vallah, Amritsar

Assistant Professor

Anubha Sharma, Department of Paediatrics, Sri Guru Ram Das Institute of Medical Sciences and Research, Vallah, Amritsar

Senior Resident

Supriya Malik, Department of Paediatrics, Sri Guru Ram Das Institute of Medical Sciences and Research, Vallah, Amritsar

Senior Resident

Downloads

Published

2016-10-22

How to Cite

Narang, G. S., Singh, T., Sharma, A., Malik, S., & Kaur, A. (2016). Association of Haemophilia with Down Syndrome. Journal of Nepal Paediatric Society, 36(1), 75–77. https://doi.org/10.3126/jnps.v36i1.11949

Issue

Section

Brief Reports/Case Reports/Case Series