Autosomal recessive inherited bleeding disorders in Pakistan: a cross-sectional study from selected regions

Autosomal recessive inherited bleeding disorders in Pakistan: a cross-sectional study from selected regions

Abstract Background Autosomal recessive bleeding disorders (ARBDs) include deficiencies of clotting factors I, II, V, VII, X, XI, XIII, vitamin K dependent clotting factors, combined factor V & VIII, Von Willebrand Disease (vWD) type 3, Glanzmann’s thrombasthenia (GT) and Bernard–Soulier syndrom...

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Bibliographic Details
Main Authors: Arshi Naz, Muhammad Younus Jamal, Samina Amanat, Ikram Din ujjan, Akber Najmuddin, Humayun Patel, Fazle Raziq, Nisar Ahmed, Ayisha Imran, Tahir Sultan Shamsi
Format: Article
Language:English
Published: BMC 2017-04-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Autosomal recessive
Inherited bleeding disorders
Coagulation factors
von Willebrand disease type 3
Glanzmann’s thrombasthenia
Bernard–Soulier syndrome
Online Access:http://link.springer.com/article/10.1186/s13023-017-0620-6

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http://link.springer.com/article/10.1186/s13023-017-0620-6

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