Hemophilia A history and symptoms: Difference between revisions

Jump to navigation Jump to search
Fahd Yunus (talk | contribs)
Fahd Yunus (talk | contribs)
Line 11: Line 11:


==Symptoms==
==Symptoms==
Mild hemophilia is usually asymptomatic, unless the patient experiences an injury or undergoes surgery. Young males often experience excessive bleeding with circumcision, or following dental procedures.
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:
* [[Joint]]s
* [[Joint]]s
Line 25: Line 26:
*Spontaneous bleeding
*Spontaneous bleeding


The muscle and joint [[Bleeding|hemorrhages]] are quite typical of hemophilia, while digestive tract and cerebral hemorrhages are also germane to other coagulation disorders.
The muscle and joint [[Bleeding|hemorrhages]] are quite typical of hemophilia, while digestive tract and cerebral hemorrhages are also germane to other coagulation disorders. Bleeding into large joints or muscles is the most common site of bleeding in hemophilia. Most common muscle bleeds include the muscles of the upper arm and forearm, the iliopsoas muscle, the thigh and the calf. Most joint bleeds affect the knees, ankles or elbows. Patients may present with pain in these areas, or they may simply present with incidental bruising or swelling. Repeated episodes of bleeds into joints may result in arthritis, and eventual destruction of cartilage in joint space.
Though uncommon, spontaneous or traumatic intracranial hemorrhages are the most catastrophic complication of hemophilia. Patients with intracranial hemorrhages present with typical symptoms, including nausea, headache, vomiting, and altered mental status. This is a medical emergency.


==References==
==References==

Revision as of 21:57, 29 July 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

Electrocardiogram

X Ray

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Hemophilia A history and symptoms On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Hemophilia A history and symptoms

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Hemophilia A history and symptoms

CDC on Hemophilia A history and symptoms

Hemophilia A history and symptoms in the news

Blogs on Hemophilia A history and symptoms

Directions to Hospitals Treating Hemophilia A

Risk calculators and risk factors for Hemophilia A history and symptoms

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

Please help WikiDoc by adding content here. It's easy! Click here to learn about editing.

Overview

History

A family history of abnormal bleeding is often present and highly suggestive of hemophilia A, though it is not essential for diagnosis

Symptoms

Mild hemophilia is usually asymptomatic, unless the patient experiences an injury or undergoes surgery. Young males often experience excessive bleeding with circumcision, or following dental procedures. 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. Bleeding into large joints or muscles is the most common site of bleeding in hemophilia. Most common muscle bleeds include the muscles of the upper arm and forearm, the iliopsoas muscle, the thigh and the calf. Most joint bleeds affect the knees, ankles or elbows. Patients may present with pain in these areas, or they may simply present with incidental bruising or swelling. Repeated episodes of bleeds into joints may result in arthritis, and eventual destruction of cartilage in joint space. Though uncommon, spontaneous or traumatic intracranial hemorrhages are the most catastrophic complication of hemophilia. Patients with intracranial hemorrhages present with typical symptoms, including nausea, headache, vomiting, and altered mental status. This is a medical emergency.

References

Template:WH Template:WS