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keratosis follicularis spinulosa decalvans, autosomal dominant (KFSD) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

keratosis follicularis spinulosa decalvans, autosomal dominant

MONDO:0013018

Also known as:KFSD

Overview

GeneticsAutosomal dominant

ResearchLimited published research (1 article)

Clinical Presentation

Built from Human Phenotype Ontology (HPO) phenotype annotations and GeneReviews clinical descriptions. Features represent findings documented across known cases — not an exhaustive list of possible symptoms.

Features include very common findings: Scarring alopecia of scalp, Sparse eyebrow, Keratosis pilaris, and Sparse eyelashes; and common findings: Keratitis, Facial erythema, Folliculitis, and Conjunctivitis and others. 18 total HPO annotations.

Organ System	Phenotype Count	Example Features
Skin	6	Alopecia, Scarring alopecia of scalp, Nail dysplasia

Prognosis

Phenotype severity distribution: 4 very common features, 7 common features.

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 keratosis follicularis spinulosa decalvans, autosomal dominant.

1 publication has been identified in PubMed for keratosis follicularis spinulosa decalvans, autosomal dominant. Research spans Case Report / Case Series (100%).

Recent Publications

Pandapatan AT (2024). [PMID: 39431258](https://pubmed.ncbi.nlm.nih.gov/39431258/). *Acta Med Philipp*. [Case Report / Case Series]

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 9:50 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:612843

GARD

Genetic and Rare Diseases Info Center

GARD:15586

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
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keratosis follicularis spinulosa decalvans, autosomal dominant

Overview

Clinical Presentation

Prognosis

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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