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Clinical Phenotype and Genetic Mutation Analysis of Nagashima-Type Palmoplantar Keratosis

Clinical Phenotype and Genetic Mutation Analysis of Nagashima-Type Palmoplantar Keratosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116192
Enrollment
Unknown
Registered
2026-01-06
Start date
2025-07-26
Completion date
Unknown
Last updated
2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clinically, NPPK primarily presents as well-demarcated, diffuse erythema and non-mutilating hyperkeratosis on the palms and soles. A characteristic finding is the development of whitish swelling upon exposure to water. The lesions may extend beyond the palmar-plantar regions to the dorsal aspects of the hands and feet, the flexor wrists, ankles, and Achilles tendon areas. Involvement of the elbows

Interventions

Observation group:None

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Regardless of age or sex; 2.Patients with a confirmed diagnosis of NPPK and their families who participate in the information collection and verification for this project; 3.The patient or their legal guardian understood the nature of the study and signed the informed consent form (ICF). In cases where the patient was unable to sign, the form was signed by their legal guardian.

Exclusion criteria

Exclusion criteria: 1.NO;

Design outcomes

Primary

MeasureTime frame
Proportion of participants with pathogenic SERPINB7 mutations;

Countries

China

Contacts

Public ContactWeilong Zhong

Peking University Shenzhen Hospital

welong1990@163.com+86 755 83923333

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026