Sickle-cell disease: Difference between revisions

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==[[Sickle-cell disease natural history|Natural History, Complications and Prognosis]]==
==[[Sickle-cell disease natural history|Natural History, Complications and Prognosis]]==


==[[Sickle-cell disease diagnosis|Diagnosis]]==
==Diagnosis==
[[Sickle-cell disease history and symptoms|History and Symptoms]] | [[Sickle-cell disease physical examination|Physical Examination]] | [[Sickle-cell disease laboratory tests|Laboratory Tests]] | [[Sickle-cell disease x ray|X-ray]] | [[Sickle-cell disease CT|CT]] | [[Sickle-cell disease MRI|MRI]] | [[ Sickle-cell disease echocardiography or ultrasound|Echocardiography or Ultrasound]] | [[Sickle-cell disease other imaging findings|Other Imaging Findings]] | [[Sickle-cell disease other diagnostic studies|Other Diagnostic Studies]]
[[Sickle-cell disease history and symptoms|History and Symptoms]] | [[Sickle-cell disease physical examination|Physical Examination]] | [[Sickle-cell disease laboratory tests|Laboratory Tests]] | [[Sickle-cell disease x ray|X-ray]] | [[Sickle-cell disease CT|CT]] | [[Sickle-cell disease MRI|MRI]] | [[ Sickle-cell disease echocardiography or ultrasound|Echocardiography or Ultrasound]] | [[Sickle-cell disease other imaging findings|Other Imaging Findings]] | [[Sickle-cell disease other diagnostic studies|Other Diagnostic Studies]]



Revision as of 20:20, 3 June 2016

Sickle cells
Sickle-shaped red blood cells
ICD-10 D57
ICD-9 282.6
OMIM 603903
DiseasesDB 1206
MedlinePlus 000527
MeSH C15.378.071.141.150.150

Sickle-cell disease Microchapters

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Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Sickle-cell disease from other Diseases

Epidemiology & Demographics

Risk Factors

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Natural History, Complications & Prognosis

Diagnosis

History & Symptoms

Physical Examination

Laboratory Findings

X Ray

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

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Treatment

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For patient information click here

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2], Aarti Narayan, M.B.B.S [3]

Synonyms and keywords: Anemia-sickle cell; hemoglobin S disease; hemoglobin SS disease; Hb SS; sickle cell anemia; SCA; drepanocytosis

Overview

Historical perspective

Classification

Pathophysiology

Causes

Differentiating Sickle-cell disease from Other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms | Physical Examination | Laboratory Tests | X-ray | CT | MRI | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies

Treatment

Medical Therapy | Prevention of Complications | Future or Investigational Therapies

References

Additional Readings

  • Chestnut, D. (1994). Perceptions of ethnic and cultural factors in the delivery of services in the treatment of sickle cell disease. Journal of Health and Social Policy, 5(3/4), 236.

External Links

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