Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Acral peeling skin syndrome (PSS) is a form of PSS characterized by superficial peeling of the skin predominantly affecting the dorsa of the hands and feet.
Features include always present findings: Cleavage at junction of stratum corneum and stratum granulosum; and common findings: Scaling skin, Erythema, Eczematoid dermatitis, and Dry, scaly skin (ichthyosis) and others. 14 total HPO annotations.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Skin | 10 | Abnormal nail morphology, Scaling skin, Erythema |
TGM5 function has not been fully characterized.
Acral peeling skin syndrome is associated with mutations in the TGM5 gene on chromosome 15.
Genetic testing for TGM5 is available. Testing is considered confirmatory for diagnosis.
Biomarker and diagnostic research for acral peeling skin syndrome has been reported in the published literature.
Phenotype severity distribution: 1 always present feature, 7 common features.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for acral peeling skin syndrome.
103 publications have been identified in PubMed for acral peeling skin syndrome. Kisho has analyzed 79 by research type. Research spans Review / Meta-Analysis (29%), Epidemiology / Natural History (19%), and Basic Science / Preclinical (14%).
Research Type | Count | % of Total |
|---|---|---|
Research summaries | 23 | 29% |
Data assembled from 6 of 12 sources · Last updated Sep 19, 2026, 6:56 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about acral peeling skin syndrome
Disease patterns and progression
15 |
19% |
Laboratory research | 11 | 14% |
Testing and diagnosis research | 8 | 10% |
Clinical study results | 8 | 10% |
Patient case studies | 7 | 9% |
New treatment approaches | 7 | 9% |
Bosnalı B (2026). [PMID: 40945129](https://pubmed.ncbi.nlm.nih.gov/40945129/). *Comput Biol Chem*. [Diagnostic / Biomarker]
Szepietowska M (2026). [PMID: 41423004](https://pubmed.ncbi.nlm.nih.gov/41423004/). *J Pediatr*. [Case Report / Case Series]
Lennon MJ (2026). [PMID: 41554956](https://pubmed.ncbi.nlm.nih.gov/41554956/). *Neuropsychopharmacology*. [Review / Meta-Analysis]
Silva V (2026). [PMID: 41498876](https://pubmed.ncbi.nlm.nih.gov/41498876/). *Arch Womens Ment Health*. [Epidemiology / Natural History]
Fang L (2026). [PMID: 42142454](https://pubmed.ncbi.nlm.nih.gov/42142454/). *Eur J Med Chem*. [Clinical Trial Publication]
Yeni ŞB (2026). [PMID: 41774465](https://pubmed.ncbi.nlm.nih.gov/41774465/). *J Biomater Sci Polym Ed*. [Review / Meta-Analysis]
Basheva-Kraeva YM (2025). [PMID: 40566617](https://pubmed.ncbi.nlm.nih.gov/40566617/). *Life (Basel)*. [Review / Meta-Analysis]
Fan J (2025). [PMID: 40990596](https://pubmed.ncbi.nlm.nih.gov/40990596/). *Pediatr Crit Care Med*. [Epidemiology / Natural History]
D'Andrea S (2025). [PMID: 40576390](https://pubmed.ncbi.nlm.nih.gov/40576390/). *J Sex Med*. [Review / Meta-Analysis]
Yin Y (2025). [PMID: 40875307](https://pubmed.ncbi.nlm.nih.gov/40875307/). *Mol Pharm*. [Epidemiology / Natural History]