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Hypotrichosis simplex type 7: A rare cause of non-syndromic woolly hair.
Indian J Dermatol Venereol Leprol
December 2024
Department of Dermatology, A.I.I.M.S, Bhubaneswar, Sijua, Patrapada, Odisha, India.
Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report.
Front Genet
January 2025
Department of Dermatology, China-Japan Friendship Hospital, Beijing, China.
Hypotrichosis simplex of the scalp (HSS) is a clinically rare monogenic autosomal dominant disorder associated with variants in the gene , which encodes the desmosome protein corneodesmosin. Although studies have reported that some medications can improve the symptoms of hair loss in HSS, there is still a lack of definitive and effective treatments for this disease. We report a familial case of HSS in an 8-year-old male child diagnosed with HSS caused by a mutation in , who was treated with botanical extracts in combination with minoxidil, which resulted in significant hair growth after two treatments.
View Article and Find Full Text PDFAutosomal recessive hereditary hypotrichosis simplex: A case report.
JAAD Case Rep
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Department of Dermatology, King Fahad General Hospital, Jeddah, Saudi Arabia.
Hereditary hypotrichosis simplex with SNRPE gene mutation.
Indian J Dermatol Venereol Leprol
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Department of Dermatology, School of Medicine, Pusan National University, Seo-Gu, Busan, Republic of Korea, Korea.
Isotretinoin-induced hair growth in a case of hereditary hypotrichosis simplex of the scalp: A promising therapeutic approach.
JAAD Case Rep
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Department of Dermatology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
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