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linear atrophoderma of Moulin - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

linear atrophoderma of Moulin

MONDO:0015371

Overview

Linear atrophoderma of Moulin (LAM) is characterized by mildly atrophic and hyperpigmented band-like lesions that follow the lines of Blaschko on the trunk or limbs. Since its initial description in 1992, less than 30 cases have been reported in the literature. Onset occurs during childhood or adolescence and the disease is non-progressive. There is no prior inflammation or subsequent scleroderma. The etiology is unknown but as LAM follows the lines of Blaschko it has been suggested that the disease is caused by mosaicism of a predisposing gene.

ResearchLimited published research (4 articles)

Prognosis

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for linear atrophoderma of Moulin.

4 publications have been identified in PubMed for linear atrophoderma of Moulin. Research spans Case Report / Case Series (100%).

Recent Publications

Hussein Al-Janabi M (2024). [PMID: 39355723](https://pubmed.ncbi.nlm.nih.gov/39355723/). *Skin Health Dis*. [Case Report / Case Series]
Ertop Doğan P (2024). [PMID: 38511542](https://pubmed.ncbi.nlm.nih.gov/38511542/). *Int J Dermatol*. [Case Report / Case Series]
Duwal A (2024). [PMID: 39369419](https://pubmed.ncbi.nlm.nih.gov/39369419/). *JNMA J Nepal Med Assoc*. [Case Report / Case Series]
Paradisi A (2024). [PMID: 38711276](https://pubmed.ncbi.nlm.nih.gov/38711276/). *J Dermatol*. [Case Report / Case Series]

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 7:50 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:140933

GARD

Genetic and Rare Diseases Info Center

GARD:19932

Questions for Your Care Team

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linear atrophoderma of Moulin

Overview

Prognosis

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team