Sickle cell anemia : Review and remedial hope

Author

Parmar, Dinesh

Source

The Egyptian Journal of Medical Human Genetics

Issue

Vol. 10, Issue 2 (30 Nov. 2009), pp.130-143, 14 p.

Publisher

Egyptian Society of Human Genetics

Publication Date

2009-11-30

Country of Publication

Egypt

No. of Pages

14

Main Subjects

Medicine

Abstract 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.

American Psychological Association (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

Modern Language Association (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

American Medical Association (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

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references : p. 139-143

Record ID

BIM-203521