نتایج جستجو برای: alopecia totalis

تعداد نتایج: 8923  

Journal: :Skin 2022

Background: Alopecia areata (AA) is an autoimmune disease characterized by nonscarring hair loss. Extensive forms of AA include alopecia totalis (AT; complete scalp loss) or universalis (AU; scalp, face, and body loss). Limited information exists about the cost healthcare burden AT AU. Methods: Using a large US administrative claims database, two mutually exclusive patient cohorts were identifi...

2012
Mohammad Ali Nilforoushzadeh Gelavizh Keshtmand Fariba Jaffary Abbas Kheirkhah

Diphencyprone (DCP) is a contact sensitizer which is used to treat dermatological disorders with an immunological origin, such as extensive alopecia areata (AA). Vitiligo is a rare but known side effect of DPCP therapy which is formed in the treatment site or remote areas. In this paper a 37-year-old man developed alopecia totalis with loss of eyebrows and eyelashes who presented some vitiligo ...

2006
A SAVIN

Percival GH. An introduction to dermatology. Edinburgh: Livingstone, 1967. 2 Pillsbury DM, Shelley WB, Kligman AM. Dermatology. Philadelphia: W B Saunders, 1956. 3 Betterle C, Peserico A, Del Prete G, Trisotto A. Autoantibodies in alopecia areata. Arch Dermatol 1975;111 :927. 4 Safai B. Alopecia areata. In: Safai B, Good RA, eds. Immunodermatology. New York: Plenum Medical Book Company, 1981:35...

Journal: :Acta dermato-venereologica 2013
Takako Yamakoshi Tsugunobu Andoh Teruhiko Makino Yasushi Kuraishi Tadamichi Shimizu

Alopecia areata (AA) is commonly characterized by patchy areas of hair loss on the scalp. AA has been considered as a tissue-specific and T cell-mediated autoimmune disease of the hair follicles with a genetic predisposition to hair loss (1, 2). Patients with AA sometimes report experiencing itch on the scalp at the same time as an increase in hair loss activity. However, the relationship betwe...

Journal: :Human molecular genetics 2015
Huijun Wang Xu Cao Zhimiao Lin Mingyang Lee Xinying Jia Yali Ren Lanlan Dai Liping Guan Jianguo Zhang Xuan Lin Jie Zhang Quan Chen Cheng Feng Eray Yihui Zhou Jinghua Yin Guiwen Xu Yong Yang

Keratoderma-hypotrichosis-leukonychia totalis syndrome (KHLS) is an extremely rare, autosomal-dominant disorder characterized by severe skin hyperkeratosis, congenital alopecia and leukonychia totalis. The genetic defect underlying KHLS remained undetermined. By performing whole-exome sequencing in a family with KHLS, we identified a heterozygous mutation (c.23G>T [p.Gly8Val]) in GJA1, which co...

Journal: :Proceedings of the Royal Society of Medicine 1931

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