Hemophilia A history and symptoms: Difference between revisions

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==Overview==
==Overview==
==History==
==History==
A [[Family history (medicine)|family history]] is frequently present, although not essential.
A [[Family history (medicine)|family history]] is frequently present, although not essential.
==Symptoms==
==Symptoms==
Hemophilia leads to a severely increased risk of bleeding from common injuries. The sites of bleeding are:
Hemophilia leads to a severely increased risk of bleeding from common injuries. The sites of bleeding are:
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[[Category:Disease]]
[[Category:Hematology]]
[[Category:Hematology]]
[[Category:Pediatrics]]
[[Category:Pediatrics]]
[[Category:Needs content]]

Revision as of 18:26, 17 June 2016

Hemophilia A Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Hemophilia A from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

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MRI

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Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

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Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

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Case #1

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

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Overview

History

A family history is frequently present, although not essential.

Symptoms

Hemophilia leads to a severely increased risk of bleeding from common injuries. The sites of bleeding are:

Other symptoms include:

The muscle and joint hemorrhages are quite typical of hemophilia, while digestive tract and cerebral hemorrhages are also germane to other coagulation disorders.

References

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