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Diseases » Familial primary cryofibrinogenemia » Introduction

Familial primary cryofibrinogenemia

Familial primary cryofibrinogenemia:

Familial primary cryofibrinogenemia: Introduction

Familial primary cryofibrinogenemia: A rare inherited disorder where exposure to cold causes various symptoms due to the presence of cryofibrinogen in the blood which precipitates when exposed to cold. More detailed information about the symptoms, causes, and treatments of Familial primary cryofibrinogenemia is available below.

Symptoms of Familial primary cryofibrinogenemia

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Painful purpura after exposure to cold
Small slow-healing skin ulcers after exposure to cold
Swollen feet after exposure to cold
Blood clots
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Home Diagnostic Testing

Home medical testing related to Familial primary cryofibrinogenemia:

Fatigue: Related Home Tests:
- Home Anemia Tests
- Home Thyroid Gland Function Tests
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Wrongly Diagnosed with Familial primary cryofibrinogenemia?

Misdiagnosis of Familial primary cryofibrinogenemia

Causes of Familial primary cryofibrinogenemia

Misdiagnosis and Familial primary cryofibrinogenemia

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, but often fails to be correctly diagnosed....read more »

Familial primary cryofibrinogenemia: Research Doctors & Specialists

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Blood Health Specialists (Hematology):
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Familial primary cryofibrinogenemia: Animations

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Familial primary cryofibrinogenemia: Broader Related Topics

Types of Familial primary cryofibrinogenemia

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