Evidence map›Paper›PMID 40282419›Full record

ArticleGenes2025

Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic

Elizabeth Phillippi, Marcelo Melo, Kelly N Messingham, Hatem El-Shanti

Abstract read
In one paragraph

Article in Genes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Elizabeth PhillippiDepartment of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0003-3270-7564
Marcelo MeloDepartment of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Kelly N MessinghamDepartment of Dermatology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0003-4630-0722
Hatem El-ShantiDepartment of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0001-6230-8316

Funding

University of Iowa Stead Family Children's Hospital 2022-2023University of Iowa Stead Family Children's Hospital 2023-2024
6 · The paper itself

Abstract

backgroundLoose anagen hair syndrome is a recently described genetic form of non-scarring alopecia that occurs in children and is due to poorly anchored hair shafts during the anagen phase. It can occur alone or in association with hair pathology or complex systemic phenotypes.

methodsWe report a mother and daughter with loose anagen hair syndrome that is associated with wooly hair, although it shows variable expressivity. We studied the family using genomic sequencing and identified an intronic variant in their

resultsWe provide experimental evidence that the identified intronic variant affects splicing in the tail domain, which is critical to the biomechanical properties of the keratin intermediate filaments. We demonstrate that it affects splicing by adding 12 bases to the mature transcript and consequently four amino acids to the peptide.

conclusionWe suspect that this variant is responsible for the poorly anchored and finely curled hair in the mother and daughter, which leads to a proposed diagnosis of autosomal dominant wooly hair, as well as loose anagen hair syndrome. We thus expand the variant spectrum of

Indexed as

Keratin-1Loose Anagen Hair SyndromeFemaleHairHeterozygoteHumansIntronsMutationPedigreePhenotypeRNA SplicingKeratin-1Keratin71keratin intermediate filamentKRT71loose anagen hair syndromeminigenewooly hair

Identifiers

PMID40282419
PMCPMC12027166

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.