Sickle cell anemia : Review and remedial hope

المؤلف

Parmar, Dinesh

المصدر

The Egyptian Journal of Medical Human Genetics

العدد

المجلد 10، العدد 2 (30 نوفمبر/تشرين الثاني 2009)، ص ص. 130-143، 14ص.

الناشر

الجمعية المصرية للأمراض الوراثية

تاريخ النشر

2009-11-30

دولة النشر

مصر

عدد الصفحات

14

التخصصات الرئيسية

الطب البشري

الملخص EN

Genetic diseases and disabilities have been described as the most ubiquitous and burdensome to the populations.

The hereditary anemia especially due to sickle cell is common globally with variably high prevalence in indigenous populations.

In India, several endogamous tribal pockets that have been malaria endemic harbor sickle cell gene in strikingly high frequency.

In this background management of sickle cell patients in context of contemporary health care system remains limited and requires integration of appropriate strategies into the existing health care delivery system.

This may involve research, diagnosis, training, genetic counseling and possible remedial interventions for urban as well as rural populations.

Remedial interventions that are possible in existing health care delivery system and potential therapies under investigation have been discussed.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Parmar, Dinesh. 2009. Sickle cell anemia : Review and remedial hope. The Egyptian Journal of Medical Human Genetics،Vol. 10, no. 2, pp.130-143.
https://search.emarefa.net/detail/BIM-203521

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Parmar, Dinesh. Sickle cell anemia : Review and remedial hope. The Egyptian Journal of Medical Human Genetics Vol. 10, no. 2 (Nov. 2009), pp.130-143.
https://search.emarefa.net/detail/BIM-203521

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Parmar, Dinesh. Sickle cell anemia : Review and remedial hope. The Egyptian Journal of Medical Human Genetics. 2009. Vol. 10, no. 2, pp.130-143.
https://search.emarefa.net/detail/BIM-203521

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 139-143

رقم السجل

BIM-203521