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Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for IFAP syndrome.
8 publications have been identified in PubMed for IFAP syndrome. Research spans Basic Science / Preclinical (50%), Review / Meta-Analysis (25%), and Other (13%).
Slater BA (2026). [PMID: 41492963](https://pubmed.ncbi.nlm.nih.gov/41492963/). *Clin Genet*. [Review / Meta-Analysis]
Butovich IA (2026). [PMID: 41130335](https://pubmed.ncbi.nlm.nih.gov/41130335/). *Exp Eye Res*. [Basic Science / Preclinical]
Kumar S (2026). [PMID: 41974659](https://pubmed.ncbi.nlm.nih.gov/41974659/). *Hum Genome Var*. [Basic Science / Preclinical]
Iwaki T (2026). [PMID: 41980932](https://pubmed.ncbi.nlm.nih.gov/41980932/). *Hum Genome Var*. [Basic Science / Preclinical]
Ishii N (2025). [PMID: 38992317](https://pubmed.ncbi.nlm.nih.gov/38992317/). *Int J Dermatol*. [Other]
Ghaznavi A (2025). [PMID: 41458897](https://pubmed.ncbi.nlm.nih.gov/41458897/). *Clin Cosmet Investig Dermatol*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Nov 4, 2026, 9:33 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about IFAP syndrome
Butovich IA (2025). [PMID: 40778116](https://pubmed.ncbi.nlm.nih.gov/40778116/). *medRxiv*. [Basic Science / Preclinical]
Zhang J (2024). [PMID: 39912473](https://pubmed.ncbi.nlm.nih.gov/39912473/). *Eur J Dermatol*. [Review / Meta-Analysis]
AI-curated news mentioning IFAP syndrome
Updated Oct 7, 2026
A new publication explores the progression from collodion membrane to alopecia in patients with IFAP/BRESHECK syndrome. This research provides insights into the underlying mechanisms of this rare genetic condition.