TLDR Loose anagen hair syndrome may be caused by keratin gene mutations.
The study explored whether Loose Anagen Hair Syndrome (LAHS) was a keratin disorder by examining 17 patients, with molecular analyses on 9 patients and their families. It identified a mutation, E337K, in the K6HF keratin gene in 3 families, suggesting a possible link to LAHS and a dominant inheritance pattern with variable penetrance. However, the study did not conclusively link LAHS to keratin mutations, indicating that other genetic factors might be involved. It also noted associated conditions like hypodontia and atopic dermatitis, and suggested that defects in the inner root sheath or companion layer could affect hair anchorage. The study highlighted the need for further research to fully understand the genetic basis of LAHS.
91 citations
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December 2000 in “The journal of cell biology/The Journal of cell biology” Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.
139 citations
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December 1998 in “The journal of investigative dermatology/Journal of investigative dermatology” K6hf is a unique protein found only in a specific layer of hair follicles.
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September 1997 in “PubMed” Loose anagen hair can appear at any age and may improve over time.
175 citations
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August 1997 in “Nature Genetics”
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April 1995 in “Clinical Genetics” Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.
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October 1992 in “Archives of Dermatology” Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.
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February 1989 in “Journal of The American Academy of Dermatology” Children with loose anagen hair have easily pluckable hair due to root sheath problems, and it might improve without treatment.