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Bazex-Dupre-Christol syndrome

Bazex-Dupre-Christol syndrome: Introduction

Bazex-Dupre-Christol syndrome: A very rare syndrome characterized by decreased hair growth, basal cell cancers and destruction of skin follicles which tends to affect the extremities, elbows and knees. More detailed information about the symptoms, causes, and treatments of Bazex-Dupre-Christol syndrome is available below.

Symptoms of Bazex-Dupre-Christol syndrome

See full list of 8 symptoms of Bazex-Dupre-Christol syndrome

Bazex-Dupre-Christol syndrome: Complications

Read more about complications of Bazex-Dupre-Christol syndrome.

Evidence Based Medicine Research for Bazex-Dupre-Christol syndrome

Medical research articles related to Bazex-Dupre-Christol syndrome include:

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Videos for Bazex-Dupre-Christol syndrome

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Reseach about Bazex-Dupre-Christol syndrome

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Stories from Users Related to Bazex-Dupre-Christol syndrome

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Definitions of Bazex-Dupre-Christol syndrome:

A syndrome combining major characteristics of the nevoid basal-cell carcinoma syndrome (qv) with follicular atrophoderma, hypotrichosis, hypohidrosis, and minor skin defects. Some patients are retarded. - (Source - Diseases Database)

Bazex-Dupre-Christol syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Bazex-Dupre-Christol syndrome, or a subtype of Bazex-Dupre-Christol 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 Bazex-Dupre-Christol syndrome as a "rare disease".
Source - Orphanet


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