Ermine phenotype
Ermine phenotype: Introduction
Ermine phenotype: A very rare syndrome characterized by pigmentation abnormalities as well as deafness.
More detailed information about the symptoms,
causes, and treatments of Ermine phenotype is available below.
Symptoms of Ermine phenotype
See full list of 8
symptoms of Ermine phenotype
Home Diagnostic Testing
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Wrongly Diagnosed with Ermine phenotype?
Ermine phenotype: Complications
Read more about complications of Ermine phenotype.
Causes of Ermine phenotype
Read more about causes of Ermine phenotype.
Misdiagnosis and Ermine phenotype
Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer
from the skin disorder called psoriasis can often go...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 estimate that about 1 per 100...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 Ermine phenotype
Ermine phenotype: Research Doctors & Specialists
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Ermine phenotype: Animations
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Statistics for Ermine phenotype
Ermine phenotype: Broader Related Topics
Types of Ermine phenotype
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Definitions of Ermine phenotype:
Ermine phenotype is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Ermine phenotype, or a subtype of Ermine phenotype,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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