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Living with Follicular atrophoderma and basal cell epitheliomata

A rare inherited skin condition (Bazex-Dupre-Christol syndrome) with a tendency to develop basal cell skin cancers early in life.

Understanding Follicular atrophoderma and basal cell epitheliomata

Follicular atrophoderma and basal cell epitheliomata, or Bazex-Dupre-Christol syndrome, is a rare hereditary skin disease.

People with it are prone to developing basal cell carcinomas, a common type of skin cancer, at an early age.

Signs & symptoms

GARD lists these among the less common findings, and we don't have enough information about how common they are:

  • Early basal cell skin cancers
  • Trichoepithelioma (hair-follicle skin growth)
  • Eczema
  • Atopic dermatitis
  • Acne inversa

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Specialists who may be involved include cancer specialists, genetic specialists and skin, hair, and nail specialists.

  3. Ask which tests can help

    Your care team will decide which exams and tests can confirm the diagnosis.

Care & treatment

Care team
Cancer specialists (oncologists); Genetic specialists (geneticists); Skin, hair, and nail specialists (dermatologists)
Expert care
Ask about multidisciplinary care centers for rare conditions
Treatment
GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
Research
Clinical trials and observational studies may be options. See the research section below.

General information, not medical advice. Your care team makes the decisions.

Everyday life

Living with a rare condition is easier with support.

  • Connect with Children's Skin Disease Foundation
  • Keep notes on symptoms, changes and questions for appointments
  • Ask about patient registries that help research
  • Look into financial aid and travel resources for care visits
Bring these questions to your next doctor visit
How often should my skin be checked by a dermatologist?
How can I protect my skin from new skin cancers?
Is genetic testing available for my family?

Quick facts

InheritanceX-Linked

Changes in genes cause it. It is X-linked, which means the gene is on the X chromosome. GARD doesn't name the gene.

GeneticSkin

Also known as: acrokeratosis of bazex; acrokeratosis paraneoplastica; acrokeratosis paraneoplastica of bazex; bazex syndrome; bazex syndrome, x-linked dominant; bazex-dupre-christol syndrome

Patient organizations

Broader rare-disease groups

Source: NIH GARD · Follicular atrophoderma and basal cell epitheliomataGARD ID 838 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with Follicular atrophoderma and basal cell epitheliomata.

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Explore research for Follicular atrophoderma and basal cell epitheliomata

Explore actively recruiting Follicular atrophoderma and basal cell epitheliomata studies with HealthSpark.

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Find actively recruiting studies for Follicular atrophoderma and basal cell epitheliomata with HealthSpark. Share your city to explore research near you.

  • Recruiting studies from ClinicalTrials.gov
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  • Eligibility is confirmed by the study team

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