Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Atp2c1 gene"'
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 7 (2024)
Externí odkaz:
https://doaj.org/article/5f51c073a7254513a81caaeaa823e16d
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Hailey–Hailey disease (HHD) is a rare autosomal-dominant blistering disorder characterized by recurrent vesicular and erosive lesions at intertriginous sites. We described a 24-year-old male who presented with multiple bright red verrucous papules
Externí odkaz:
https://doaj.org/article/526367dc4b4945fdb294b8ad20b2fecb
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Abstract Background Hailey–Hailey disease (HHD; OMIM: 169600) is an autosomal dominate genodermatosis, characterized by recurrent blisters and erosions clinically and remarkable acantholysis pathologically. The underlying pathogenic factor is the m
Externí odkaz:
https://doaj.org/article/26cfa182a19f4744845d4674415515c2
Akademický článek
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Publikováno v:
Саратовский научно-медицинский журнал, Vol 11, Iss 3, Pp 442-444 (2015)
The study presents a relatively rare case of dermatosis. It is familial benign chronic vesicular fever (Hailey-Hailey disease) in a 58-years old female patient which is inherited as an autosomal dominant mode. The data about etiology, pathogenesis, c
Externí odkaz:
https://doaj.org/article/43f03173b31b4b1c9e9eb81ecca9fa48
Publikováno v:
Dermatologica Sinica, Vol 28, Iss 2, Pp 59-63 (2010)
Background: Hailey-Hailey disease (HHD) is an autosomal dominant disorder with recurrent pruritic vesicles and erosions, and scaly erythematous plaques, particularly involving intertriginous areas such as the neck, axillae, groins and perineum. Histo
Externí odkaz:
https://doaj.org/article/cfeffe41b274476f8db9cb3c410bbe69
Publikováno v:
Medicina Cutánea Ibero-Latino-Americana. 47:200-204
espanolLa enfermedad de Hailey-Hailey (penfigo benigno familiar) es una genodermatosis debida a la mutacion en el gen ATP2C1, caracterizada por la aparicion de vesiculas flacidas que comprometen principalmente la zona de pliegues y en su evolucion se
Publikováno v:
The Journal of Dermatology. 48
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Hailey–Hailey disease (HHD; OMIM: 169600) is an autosomal dominate genodermatosis, characterized by recurrent blisters and erosions clinically and remarkable acantholysis pathologically. The underlying pathogenic factor is the mutation o
Publikováno v:
SAGE Open Medical Case Reports, Vol 8 (2020)
SAGE Open Medical Case Reports
SAGE Open Medical Case Reports
Hailey–Hailey disease is a rare autosomal dominant acantholytic disorder due to mutation in the ATP2C1 gene and presents with flaccid blisters in intertriginous regions. Its chronic and relapsing course may negatively impact patients’ quality of