Sickle cell anemia: An update on diagnosis, management and prevention strategies

Sickle cell anemia is the most common disease entity of all the monogenic disorders. This is an autosomal recessive disorder. HbS polymerization, vaso-occlusion, and hemolytic anemia are central to the pathophysiology of sickle cell disease, they precipitate a cascade of pathologic events, which in...

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Published in:Indian Journal of Community and Family Medicine
Main Authors: Shruti Mishra, Gaurav Chhabra
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Subjects:
Online Access:http://www.ijcfm.org/article.asp?issn=2395-2113;year=2018;volume=4;issue=2;spage=67;epage=71;aulast=Mishra
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author Shruti Mishra
Gaurav Chhabra
author_facet Shruti Mishra
Gaurav Chhabra
author_sort Shruti Mishra
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container_title Indian Journal of Community and Family Medicine
description Sickle cell anemia is the most common disease entity of all the monogenic disorders. This is an autosomal recessive disorder. HbS polymerization, vaso-occlusion, and hemolytic anemia are central to the pathophysiology of sickle cell disease, they precipitate a cascade of pathologic events, which in turn lead to a wide range of complications. The disease is particularly more prevalent in certain regions of the country like Odisha, Madhya Pradesh, Tamilnadu and has a significant impact on morbidity. Community based approach by providing availability of screening tests, & pre-marital and pre-pregnancy counselling should be initiated to reduce the disease burden in the society.
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spelling doaj-art-3ee3fd79b44f4671bc7acaaeb7501bd12025-08-19T21:30:18ZengWolters Kluwer Medknow PublicationsIndian Journal of Community and Family Medicine2395-21132018-01-0142677110.4103/2395-2113.251444Sickle cell anemia: An update on diagnosis, management and prevention strategiesShruti MishraGaurav ChhabraSickle cell anemia is the most common disease entity of all the monogenic disorders. This is an autosomal recessive disorder. HbS polymerization, vaso-occlusion, and hemolytic anemia are central to the pathophysiology of sickle cell disease, they precipitate a cascade of pathologic events, which in turn lead to a wide range of complications. The disease is particularly more prevalent in certain regions of the country like Odisha, Madhya Pradesh, Tamilnadu and has a significant impact on morbidity. Community based approach by providing availability of screening tests, & pre-marital and pre-pregnancy counselling should be initiated to reduce the disease burden in the society.http://www.ijcfm.org/article.asp?issn=2395-2113;year=2018;volume=4;issue=2;spage=67;epage=71;aulast=Mishrasickle cell anemiasickle cell diseasesickle cell anemia diagnosissickle cell anemia management.
spellingShingle Shruti Mishra
Gaurav Chhabra
Sickle cell anemia: An update on diagnosis, management and prevention strategies
sickle cell anemia
sickle cell disease
sickle cell anemia diagnosis
sickle cell anemia management.
title Sickle cell anemia: An update on diagnosis, management and prevention strategies
title_full Sickle cell anemia: An update on diagnosis, management and prevention strategies
title_fullStr Sickle cell anemia: An update on diagnosis, management and prevention strategies
title_full_unstemmed Sickle cell anemia: An update on diagnosis, management and prevention strategies
title_short Sickle cell anemia: An update on diagnosis, management and prevention strategies
title_sort sickle cell anemia an update on diagnosis management and prevention strategies
topic sickle cell anemia
sickle cell disease
sickle cell anemia diagnosis
sickle cell anemia management.
url http://www.ijcfm.org/article.asp?issn=2395-2113;year=2018;volume=4;issue=2;spage=67;epage=71;aulast=Mishra
work_keys_str_mv AT shrutimishra sicklecellanemiaanupdateondiagnosismanagementandpreventionstrategies
AT gauravchhabra sicklecellanemiaanupdateondiagnosismanagementandpreventionstrategies