Tietz syndrome: Introduction
Tietz syndrome: Tietz syndrome is a relatively rare condition characterized by deafness and albinism. It should not be confused with the similarly named Tietz's syndrome which involves inflammation of chest cartilage.
More detailed information about the symptoms,
causes, and treatments of Tietz syndrome is available below.
Symptoms of Tietz syndrome
See full list of 8
symptoms of Tietz syndrome
Home Diagnostic Testing
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Wrongly Diagnosed with Tietz syndrome?
Tietz syndrome: Related Patient Stories
Causes of Tietz syndrome
- The condition is caused by a chromosomal anomaly and is inherited in an autosomal dominant manner
- more causes...»
Read more about causes of Tietz syndrome
More information about causes of Tietz syndrome:
Misdiagnosis and Tietz syndrome
Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer
from the skin disorder called psoriasis can often go undiagnosed.
The main problem is that...read more »
Rare form of hair loss often misdiagnosed: a rare form of
extreme hair loss called "Atrichia with papular lesions" (APL) is often misdiagnosed
as alopecia totalis.
Researchers...read more »
Hair and scalp disorders misdiagnosed in African Americans: A higher than average
percentage of misdiagnoses of hair or scalp disorders seem to occur in African Americans.
Some of the...read more »
Read more about Misdiagnosis and Tietz syndrome
Tietz syndrome: Research Doctors & Specialists
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Tietz syndrome: Animations
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Statistics for Tietz syndrome
Tietz syndrome: Broader Related Topics
Types of Tietz syndrome
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Definitions of Tietz syndrome:
Tietz syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Tietz syndrome, or a subtype of Tietz 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 Tietz syndrome as a "rare disease".
Source - Orphanet
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