Unusual Clinical Presentation of Autosomal Recessive Woolly Hair
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Published:2020
Issue:2
Volume:6
Page:120-122
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ISSN:2296-9195
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Container-title:Skin Appendage Disorders
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language:en
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Short-container-title:Skin Appendage Disord
Author:
Alsharif Osama, Ahmed Azhar Abbas, Alali Azhar MohammedORCID, Kaki Adnan Ahmed
Reference7 articles.
1. Horev L, Tosti A, Rosen I, Hershko K, Vincenzi C, Nanova K, et al. Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair. J Am Acad Dermatol. 2009 Nov;61(5):813–8. German. 2. Zernov NV, Skoblov MY, Marakhonov AV, Shimomura Y, Vasilyeva TA, Konovalov FA, et al. Autosomal recessive hypotrichosis with woolly hair caused by a mutation in the keratin 25 gene expressed in hair follicles. J Invest Dermatol. 2016 Jun;136(6):1097–105. 3. Takeichi T, Tanahashi K, Taki T, Kono M, Sugiura K, Akiyama M. Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan. Br J Dermatol. 2017 Jul;177(1):290–2. 4. Itoh E, Nakahara T, Furumura M, Furue M, Shimomura Y. Case of autosomal recessive woolly hair/hypotrichosis with atopic dermatitis. J Dermatol. 2017 Oct;44(10):1185–6. 5. Shimomura Y, Wajid M, Zlotogorski A, Lee YJ, Rice RH, Christiano AM. Founder mutations in the lipase H gene in families with autosomal recessive woolly hair/hypotrichosis. J Invest Dermatol. 2009 Aug;129(8):1927–34.
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