Fechtner syndrome

Introduction: Fechtner syndrome

Description of Fechtner syndrome

Fechtner syndrome (medical condition): A rare condition characterized by the presence of large blood platelets, kidney inflammation, deafness and abnormal leukocytes.

See also:

Fechtner syndrome:
  »Introduction: Fechtner syndrome
  »Symptoms of Fechtner syndrome

Fechtner syndrome: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Fechtner syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Fechtner syndrome, or a subtype of Fechtner syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Fechtner syndrome as a "rare disease".

Source - Orphanet

Fechtner syndrome as a Disease

Fechtner syndrome (medical condition): See Fechtner syndrome (disease information).
  »Introduction: Fechtner syndrome
  »Symptoms of Fechtner syndrome

More information on medical condition: Fechtner syndrome:

• Information about Fechtner syndrome
• Basic Summary for Fechtner syndrome
• Symptoms of Fechtner syndrome
• Complications of Fechtner syndrome

Terms associated with Fechtner syndrome:

Terms Similar to Fechtner syndrome:

• Fechtner's syndrome
• Macrothrombocytopathy, nephritis, deafness, and leukocyte inclusions
• Variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia

Source - NIH

External links related to: Fechtner syndrome

• OMIM - FECHTNER SYNDROME; FTNS

Source: Diseases Database

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Medical dictionaries:

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