Guidelines for screening, diagnosis and management of hemoglobinopathies.

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dc.contributor.authorGhosh, Kanjaksha
dc.contributor.authorColah, Roshan
dc.contributor.authorManglani, Mamta
dc.contributor.authorChoudhry, Ved Prakash
dc.contributor.authorVerma, Ishwar
dc.contributor.authorMadan, Nishi
dc.contributor.authorSaxena, Renu
dc.contributor.authorJain, Dipty
dc.contributor.authorMarwaha, Neelam
dc.contributor.authorDas, Reena
dc.contributor.authorMohanty, Dipika
dc.contributor.authorChoudhary, Rajendra
dc.contributor.authorAgarwal, Sarita
dc.contributor.authorGhosh, Malay
dc.contributor.authorRoss, Cecil
dc.date.accessioned2015-03-09T08:19:51Z
dc.date.available2015-03-09T08:19:51Z
dc.date.issued2014-04
dc.description.abstractThe b‑thalassemias and sickle cell disorders are a major health burden in India. Diagnosis and management of these disorders both in adults and in newborns using appropriate approaches and uniform technology are important in different regions of a vast and diverse country as India. In view of a National Thalassemia Control Program to be launched soon, a need was felt for guidelines on whom to screen, cost‑effective technologies that are to be used as well as for establishing prenatal diagnosis programs in regional centers. Newborn screening for sickle cell disorders is in its infancy in India and uniform approaches need to be followed. Also, included are guidelines for monitoring and managing patients who are now growing older and need comprehensive care as well as management of complications of the disease.en_US
dc.identifier.citationGhosh Kanjaksha, Colah Roshan, Manglani Mamta, Choudhry Ved Prakash, Verma Ishwar, Madan Nishi, Saxena Renu, Jain Dipty, Marwaha Neelam, Das Reena, Mohanty Dipika, Choudhary Rajendra, Agarwal Sarita, Ghosh Malay, Ross Cecil. Guidelines for screening, diagnosis and management of hemoglobinopathies. Indian Journal of Human Genetics. 2014 Apr-Jun ; 20 (2): 101-119.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/156647
dc.language.isoenen_US
dc.source.urihttps://www.ijhg.com/article.asp?issn=0971-6866;year=2014;volume=20;issue=2;spage=101;epage=119;aulast=Ghoshen_US
dc.subjectDiagnosisen_US
dc.subjectguidelinesen_US
dc.subjecthemoglobinopathiesen_US
dc.subjectmanagementen_US
dc.subjectsickle cell diseaseen_US
dc.subjectthalassemiaen_US
dc.subject.meshAnemia, Sickle Cell --diagnosis
dc.subject.meshAnemia Sickle Cell --therapy
dc.subject.meshHemoglobinopathies --diagnosis
dc.subject.meshHemoglobinopathies --therapy
dc.subject.meshHumans
dc.subject.meshMass Screening --methods
dc.subject.meshMass Screening --standards
dc.subject.meshNeonatal Screening --methods
dc.subject.meshNeonatal Screening --standards
dc.subject.meshPrenatal Diagnosis --methods
dc.subject.meshPrenatal Diagnosis --standards
dc.subject.meshbeta-Thalassemia --diagnosis
dc.subject.meshbeta-Thalassemia --therapy
dc.titleGuidelines for screening, diagnosis and management of hemoglobinopathies.en_US
dc.typeArticleen_US
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