Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss.

doi:10.1093/bjd/ljad314

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Article

Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss.

The British journal of dermatology - 16 Nov 2023

Cesarato Nicole, Schwieger-Briel Agnes, Gossmann Yasmina, Henne Sabrina K, Hillmann Kathrin, Frommherz Leonie H, Wehner Maria, Xiong Xing, Thiele Holger, Oji Vinzenz, Milani Donatella, Tantcheva-Poor Iliana, Giehl Kathrin, Fölster-Holst Regina, Teichler Anne, Braeckmans Delphine, Hoeger Peter H, Jones Gabriela, Frank Jorge, Weibel Lisa, Blume-Peytavi Ulrike, Hamm Henning, Nöthen Markus M, Geyer Matthias, Heilmann-Heimbach Stefanie, Basmanav F Buket, Betz Regina C

Abstract excerpt

BACKGROUND: Short anagen hair (SAH) is a rare paediatric hair disorder characterized by a short anagen phase, an inability to grow long scalp hair and a negative psychological impact. The genetic basis of SAH is currently unknown. OBJECTIVES: To perform molecular genetic investigations in 48 individuals with a clinical phenotype suggestive of SAH to identify, if any, the genetic basis of this condition. METHODS:...

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PMID: 37671665
DOI: 10.1093/bjd/ljad314

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