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Quoted phrase not found in phrase index: "Autosomal recessive congenital ichthyosis 10"
Page 1
Ichthyosis: etiology, diagnosis, and management.
DiGiovanna JJ, Robinson-Bostom L. DiGiovanna JJ, et al. Am J Clin Dermatol. 2003;4(2):81-95. doi: 10.2165/00128071-200304020-00002. Am J Clin Dermatol. 2003. PMID: 12553849 Review.
Congenital autosomal recessive ichthyosis (CARI) usually presents at birth, often as a collodion baby. CARI can progress into any one of a spectrum of disorders. Lamellar ichthyosis is characterized by dark, plate (armor)-like scale. ...
Congenital autosomal recessive ichthyosis (CARI) usually presents at birth, often as a collodion baby. CARI can …
Vitamin D: A New Promising Therapy for Congenital Ichthyosis.
Sethuraman G, Marwaha RK, Challa A, Yenamandra VK, Ramakrishnan L, Thulkar S, Sharma VK. Sethuraman G, et al. Pediatrics. 2016 Jan;137(1). doi: 10.1542/peds.2015-1313. Epub 2015 Dec 31. Pediatrics. 2016. PMID: 26721572
Seven children with congenital ichthyosis (5 with autosomal recessive congenital ichthyosis; 2 with epidermolytic ichthyosis) and severe vitamin D deficiency (and/or rickets) were given 60,000 IU of oral cholecalciferol daily for …
Seven children with congenital ichthyosis (5 with autosomal recessive congenital ichthyosis; 2 wit …
Results of a nationwide epidemiologic survey of autosomal recessive congenital ichthyosis and ichthyosis syndromes in Japan.
Kurosawa M, Uehara R, Takagi A, Aoyama Y, Iwatsuki K, Amagai M, Nagai M, Nakamura Y, Inaba Y, Yokoyama K, Ikeda S. Kurosawa M, et al. J Am Acad Dermatol. 2019 Nov;81(5):1086-1092.e1. doi: 10.1016/j.jaad.2018.07.056. Epub 2018 Sep 26. J Am Acad Dermatol. 2019. PMID: 30268591
BACKGROUND: Autosomal recessive congenital ichthyosis (ARCI) and ichthyosis syndrome (IS) are rare genetic skin disorders. ...The estimated disease distribution was as follows: 95 (95% CI 80-110) patients with nonbullous congenital ichthy …
BACKGROUND: Autosomal recessive congenital ichthyosis (ARCI) and ichthyosis syndrome (IS) are rare geneti …
Phase IIb randomized CONTROL study demonstrates a novel topical isotretinoin formulation, TMB-001, is safe and effective in participants with either recessive X-linked or autosomal recessive lamellar congenital ichthyosis.
Murrell DF, Teng JMC, Guenthner S, Marathe K, Kempers S, Eads K, Castelo-Soccio L, Mendelsohn AM, Raiz J, Bunick CG. Murrell DF, et al. Clin Exp Dermatol. 2023 Jun 5;48(6):623-630. doi: 10.1093/ced/llad033. Clin Exp Dermatol. 2023. PMID: 36794376 Clinical Trial.
BACKGROUND: In two severe congenital ichthyosis subtypes, autosomal recessive lamellar ichthyosis (ARCI-LI) and X-linked recessive ichthyosis (XLRI), cutaneous manifestations include widespread scaling. ...Most AEs were appl …
BACKGROUND: In two severe congenital ichthyosis subtypes, autosomal recessive lamellar ichthyosis …
Biologics for inherited disorders of keratinisation: A systematic review.
Chen MKY, Flanagan AL, Sebaratnam DF, Gu Y. Chen MKY, et al. Australas J Dermatol. 2024 Mar;65(2):185-214. doi: 10.1111/ajd.14197. Epub 2023 Dec 21. Australas J Dermatol. 2024. PMID: 38126177
The most common disorders were Netherton syndrome (n = 63; 38%), autosomal recessive congenital ichthyoses (n = 27; 16%), CARD14-associated papulosquamous eruptions (n = 17; 10%) and familial pityriasis rubra pilaris (PRP) (n = 15; 9%).Of the 207 times …
The most common disorders were Netherton syndrome (n = 63; 38%), autosomal recessive congenital ichthyoses (n = 27; 16% …
Use of Topical Glycolic Acid Plus a Lovastatin-Cholesterol Combination Cream for the Treatment of Autosomal Recessive Congenital Ichthyoses.
Khalil S, Bardawil T, Saade S, Chedraoui A, Ramadan N, Hasbani DJ, Abbas O, Nemer G, Rubeiz N, Kurban M. Khalil S, et al. JAMA Dermatol. 2018 Nov 1;154(11):1320-1323. doi: 10.1001/jamadermatol.2018.2904. JAMA Dermatol. 2018. PMID: 30208477 Free PMC article.
IMPORTANCE: Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of disorders caused by defects in signaling pathways involved in epidermal proliferation and differentiation, leading to a wide range of skin manifestations. ...Topic …
IMPORTANCE: Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of disorders caused by def …
Treatment of ichthyosis lamellaris using a series of herbal skin care products family.
Tirant M, Bayer P, Hercogovấ J, Fioranelli M, Gianfaldoni S, Chokoeva AA, Tchernev G, Wollina U, Novotny F, Roccia MG, Maximov GK, França K, Lotti T. Tirant M, et al. J Biol Regul Homeost Agents. 2016 Apr-Jun;30(2 Suppl 3):65-72. J Biol Regul Homeost Agents. 2016. PMID: 27498660 Clinical Trial.
Lamellar ichthyosis (LI) is a genetically heterogeneous group of disorders of keratinization that are inherited in an autosomal recessive fashion, occurring in approximately 1 in 300,000 live births. ...A multi-centre European prospective study was con …
Lamellar ichthyosis (LI) is a genetically heterogeneous group of disorders of keratinization that are inherited in an autos …
The expression of epidermal lipoxygenases and transglutaminase-1 is perturbed by NIPAL4 mutations: indications of a common metabolic pathway essential for skin barrier homeostasis.
Li H, Loriè EP, Fischer J, Vahlquist A, Törmä H. Li H, et al. J Invest Dermatol. 2012 Oct;132(10):2368-2375. doi: 10.1038/jid.2012.160. Epub 2012 May 24. J Invest Dermatol. 2012. PMID: 22622417 Free article.
Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of skin barrier diseases due inter alia to mutations in transglutaminase-1 (TGM1), in lipoxygenases (LOXs) of the hepoxilin pathway, and in ichthyin, a putative Mg(2+) transporte …
Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of skin barrier diseases due inter ali …
Effect of topical tazarotene in the treatment of congenital ichthyoses.
Hofmann B, Stege H, Ruzicka T, Lehmann P. Hofmann B, et al. Br J Dermatol. 1999 Oct;141(4):642-6. doi: 10.1046/j.1365-2133.1999.03101.x. Br J Dermatol. 1999. PMID: 10583110
Twelve consecutive patients with different forms of congenital ichthyosis were enrolled in an open, non-randomized, intraindividually controlled, half-side pilot study. Diagnoses were X-linked recessive ichthyosis, non-erythrodermic autosomal …
Twelve consecutive patients with different forms of congenital ichthyosis were enrolled in an open, non-randomized, int …
Flow-cytometric investigation of epidermal cell characteristics in monogenic disorders of keratinization and their modulation by topical calcipotriol treatment.
Lucker GP, Steijen PM, Suykerbuyk EJ, Kragballe K, Brandrup F, van de Kerkhof PC. Lucker GP, et al. Acta Derm Venereol. 1996 Mar;76(2):97-101. doi: 10.2340/000155557697101. Acta Derm Venereol. 1996. PMID: 8740259 Free article.
Proliferation, measured by the percentage of epidermal cells in SG2M-phase of the cell cycle, was increased in Darier's disease, lamellar ichthyosis, congenital bullous ichthyotic erythroderma of Brocq and the Comel-Netherton syndrome, whereas normal prolifer …
Proliferation, measured by the percentage of epidermal cells in SG2M-phase of the cell cycle, was increased in Darier's disease, lamellar …
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