Pendred syndrome
Pendred syndrome: Introduction
Pendred syndrome:
Pendred syndrome is an inherited disorder that accounts for as much as 10% of hereditary deafness. Patients usually also suffer from thyroid goiter. The ... more about Pendred syndrome.
Pendred syndrome: An inherited condition characterized by hearing loss and goiter formation. The enlarged thyroid gland often continuges to function normally.
More detailed information about the symptoms,
causes, and treatments of Pendred syndrome is available below.
Symptoms of Pendred syndrome
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symptoms of Pendred syndrome
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Wrongly Diagnosed with Pendred syndrome?
Pendred syndrome: Related Patient Stories
Pendred syndrome: Deaths
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Pendred syndrome: Complications
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Causes of Pendred syndrome
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Disease Topics Related To Pendred syndrome
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Pendred syndrome: Research Doctors & Specialists
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Evidence Based Medicine Research for Pendred syndrome
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Pendred syndrome: Animations
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Prognosis for Pendred syndrome
Prognosis for Pendred syndrome:
goiter often recurs after surgery
More about prognosis of Pendred syndrome
Research about Pendred syndrome
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Statistics for Pendred syndrome
Pendred syndrome: Broader Related Topics
Types of Pendred syndrome
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Article Excerpts about Pendred syndrome
Pendred syndrome is an inherited disorder that accounts for as much as 10% of hereditary deafness. Patients usually also suffer from thyroid goiter. The recent discovery of the gene for Pendred syndrome illuminates a disorder that has confounded scientists for more than a century.
(Source: Genes and Disease by the National Center for Biotechnology)
Definitions of Pendred syndrome:
Pendred syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Pendred syndrome, or a subtype of Pendred syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Pendred syndrome as a "rare disease".
Source - Orphanet
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