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Living with Keratosis palmoplantaris striata 3

A genetic skin condition with patches of thick, scaly skin on the palms and soles, caused by a change in the KRT1 gene.

Understanding Keratosis palmoplantaris striata 3

Keratosis palmoplantaris striata 3 (PPKS3) is a genetic condition that causes patches of thick, scaly skin on the palms and soles.

The thick skin affects the palms of the hands and the soles of the feet. GARD does not list the age when it starts.

Signs & symptoms

GARD lists this among the most common symptoms:

  • Thick, scaly skin on the palms and soles

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

    Your doctor may refer you to a specialist who knows rare conditions.

  3. Ask which tests can help

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

  4. Connect with expert centers

    Foundation for Ichthyosis and Related Skin Types may keep lists of experts for this condition.

Care & treatment

Care team
A doctor familiar with rare conditions, plus specialists as needed
Expert care
Expert lists: Foundation for Ichthyosis and Related Skin Types
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 Foundation for Ichthyosis and Related Skin Types
  • 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
Can genetic testing for the KRT1 gene confirm the diagnosis?
What skin care helps with thick, scaly patches?
How likely is it that other family members will have it?

Quick facts

InheritanceAutosomal Dominant

A change in the keratin-1 (KRT1) gene causes this condition. It is autosomal dominant, meaning one changed copy of the gene is enough.

Also known as: keratoderma, palmoplantar, striate form iii; keratosis palmoplantaris striata iii; keratosis palmoplantaris striata type 3; krt1 striate palmoplantar keratoderma; ppks3; striate palmoplantar keratoderma caused by mutation in krt1

Patient organizations

Source: NIH GARD · Keratosis palmoplantaris striata 3GARD ID 9173 · 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 Keratosis palmoplantaris striata 3.

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