Zobrazeno 1 - 10
of 1 302
pro vyhledávání: '"congenital ichthyosis"'
Autor:
Eduard T. Ambarchyan, Anastasiya D. Kuzminova, Totuy K. Eldarova, Vladislav V. Ivanchikov, Nataliya V. Zhurkova, Nato D. Vashakmadze
Publikováno v:
Вопросы современной педиатрии, Vol 23, Iss 3, Pp 181-187 (2024)
Background. Ichthyosis follicularis with atrichia and photophobia (IFAP syndrome), type 2 is a rare hereditary disease from the group of syndromic forms of ichthyosis. It is clinically characterized by triad of non-inflammatory follicular ichthyosis,
Externí odkaz:
https://doaj.org/article/87fecd515f60437a9eed4f992bcabd47
Autor:
Ryoko Hino, Yuta Chiba, Yuriko Maruya, Manami Tadano, Shinji Otake, Seira Hoshikawa, Yoji Sasahara, Kan Saito
Publikováno v:
Frontiers in Dental Medicine, Vol 5 (2024)
Congenital ichthyosis is a disease in which the stratum corneum on the surface of the skin becomes thick from the time of the fetus and the barrier function of the skin is impaired. Congenital ichthyosis is a genetic disorder that causes ectodermal a
Externí odkaz:
https://doaj.org/article/afbdc4d3f8f743f7a1581deef754b058
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 25, Iss 2, Pp 99-106 (2024)
Objective: Ichthyosis is a disorder of cornification, which can be acquired or inherited, and encompasses various forms of generalized scaling and superficial roughness of the skin secondary to impaired skin barrier. It can be often associated with s
Externí odkaz:
https://doaj.org/article/48b1c864fc324b1abc2f5e55c63f2641
Autor:
Rahul Mahajan, Shirin Bakshi, Debajyoti Chatterjee, Dipankar De, Uma N. Saikia, Sanjeev Handa
Publikováno v:
Indian Journal of Dermatology, Vol 69, Iss 2, Pp 113-118 (2024)
Background: Congenital ichthyoses are a rare Mendelian group of disorders affecting the integument with a heterogeneous clinical presentation amongst which scaling is a constant feature. There is scanty epidemiologic data regarding the clinical profi
Externí odkaz:
https://doaj.org/article/30d95b91a3b64482a42cf10107bfe7aa
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 5, Pp n/a-n/a (2024)
Abstract Background Ichthyosis is a common keratotic skin disease with high clinical, etiological and genetic heterogeneity. There are four types of non‐syndromic hereditary ichthyoses, among which autosomal recessive congenital ichthyosis (ARCI) i
Externí odkaz:
https://doaj.org/article/d05577da968d4a2fb85ff0763d24f03f
Autor:
Karine O. Avetisyan, Nikolay N. Murashkin, Svetlana G. Makarova, Svetlana S. Petrichuk, Daria G. Kuptsova
Publikováno v:
Вопросы современной педиатрии, Vol 22, Iss 5, Pp 415-424 (2023)
Background. Congenital ichthyoses (CIs) are a heterogeneous clinical-etiological group of genodermatoses. Typical clinical symptoms of this disease, regardless of the form, are generalized erythroderma, peeling, itching, hyperkeratosis, severe struct
Externí odkaz:
https://doaj.org/article/c018c9bdf76c4ee89862a2ecde01a6ae
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 12, Iss 11, Pp 2990-2993 (2023)
The ichthyosis, also called disorders of keratinization or cornification, are heterogeneous group of disorders characterized by a generalized scaling of the skin of varying severity. The majority of ichthyosis is inherited but acquired forms can deve
Externí odkaz:
https://doaj.org/article/79e9b5bad2a14c33a8fe6d5f00f7a5f3
Autor:
Nicoleta Anton, Francesca Cristiana Dohotariu, Ruxandra Angela Pîrvulescu, Ileana Ramona Barac, Camelia Margareta Bogdănici
Publikováno v:
Biomedicines, Vol 12, Iss 10, p 2164 (2024)
We report a surgically challenging case, in the context of a diagnosis of juvenile glaucoma refractory to drug therapy, multi-operated, known patient with congenital ichthyosis, part of Dorfman–Chanarin Syndrome (DCS), with a single functional eye.
Externí odkaz:
https://doaj.org/article/54bbf73a00fd4804af1143d03491a34f
Publikováno v:
Педиатрическая фармакология, Vol 20, Iss 4, Pp 297-302 (2023)
Background. Ichthyosis is a group of rare genetic diseases with a wide phenotypic spectrum, characterized most often by generalized hyperkeratinization and desquamation with variable erythema [1]. In most cases, the diagnosis is established immediate
Externí odkaz:
https://doaj.org/article/4a1feb60ae574fc89a0b0840c188af25
Autor:
Kalyani Marathe, Joyce M. C. Teng, Scott Guenthner, Christopher G. Bunick, Steven Kempers, Kimmie Eads, Leslie Castelo-Soccio, Alan M. Mendelsohn, Jessica Raiz, Dédée F. Murrell
Publikováno v:
Dermatology and Therapy, Vol 13, Iss 6, Pp 1255-1264 (2023)
Abstract Introduction Treatment with oral retinoids can be effective in patients with congenital ichthyosis (CI) but may be associated with clinically significant laboratory changes. In this Phase 2b CONTROL study analysis, we characterize the effect
Externí odkaz:
https://doaj.org/article/0589bfedc89443abbc72105e37c33aed