April 2016 in “Journal of Investigative Dermatology” Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.
April 2024 in “The journal of investigative dermatology/Journal of investigative dermatology” ASH2L is essential for skin and hair development.
September 2001 in “Swiss Medical Forum ‒ Schweizerisches Medizin-Forum” 2 citations
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January 2000 in “Quaternary Science Reviews” January 2026 in “Journal of Cutaneous and Aesthetic Surgery” January 2019 in “Deleted Journal” April 2016 in “Annales de Dermatologie et de Vénéréologie”
May 2022 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not available.
2 citations
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August 2012 in “Journal of the American Academy of Dermatology” Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.
August 2022 in “Frontiers in genetics” A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.
The conclusion cannot be provided because the document content is not available.
June 2023 in “Antioxidants” Lipids from Schizochytrium sp. help prevent hair loss by protecting hair cells from damage and promoting hair growth.
January 1982 in “Los Cuadernos del Norte: Revista cultural de la Caja de Ahorros de Asturias” 17 citations
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May 2007 in “British Journal of Dermatology” Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.
8 citations
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November 2009 in “The Neurologist/The neurologist” If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.
January 2002 in “Agritrop (Cirad)” The hr gene is linked to hair loss in Valle del Belice sheep.
September 1998 in “British journal of plastic surgery” 1 citations
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February 2006 in “The Journal of Urology” August 2006 in “The Journal of Urology” 5 citations
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February 2005 in “Journal of the American Academy of Dermatology” Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.
January 2025 in “Turkish Journal of Cerebrovascular Diseases” CARASIL can cause different symptoms even with the same genetic mutation.
1 citations
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February 1991 in “Journal of Biological Chemistry” A skin model using hair and skin cells can mimic human skin for research.
2 citations
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January 1990 3 citations
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December 2022 in “The Neurologist” CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.
November 2007 in “The Journal of Urology”
4 citations
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June 2021 in “Dermatology” Scientists created a 3D skin model to study a chronic skin disease and test treatments.