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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 …
Harlequin Ichthyosis - A Case Report.
Ugezu CH, Mazumdar A, Dunn E, Das A. Ugezu CH, et al. Ir Med J. 2017 Aug 8;110(7):606. Ir Med J. 2017. PMID: 29341518
Harlequin Ichthyosis is a very rare genetic disorder affecting mainly the skin with severe morbidity and mortality. It affects both sexes with incidence of about 1 in 300,000 live births. Autosomal recessive inheritance has been inferred with mutation in ABCA …
Harlequin Ichthyosis is a very rare genetic disorder affecting mainly the skin with severe morbidity and mortality. It affects both s …
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
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 1 …
Seven children with congenital ichthyosis (5 with autosomal recessive congenital ichthyosis; 2 wit …
A case of harlequin ichthyosis treated with isotretinoin.
Chang LM, Reyes M. Chang LM, et al. Dermatol Online J. 2014 Feb 18;20(2):doj_21540. Dermatol Online J. 2014. PMID: 24612573 Free article.
Harlequin ichthyosis is a rare congenital ichthyosis classified under the category of Autosomal Recessive Congenital Ichthyoses, which also include lamellar ichthyosis and congenital ichthyosiform erythroderma. ...Ear …
Harlequin ichthyosis is a rare congenital ichthyosis classified under the category of Autosomal Recessive
Dorfman-Chanarin syndrome in two female siblings: a case report and discussion on approach and management.
Chander R, Varghese B, Garg T, Mittal S, Singh S. Chander R, et al. Dermatol Online J. 2011 Apr 15;17(4):7. Dermatol Online J. 2011. PMID: 21549082 Free article.
Dorfman-Chanarin syndrome (DCS) is a very rare disorder of lipid metabolism that exhibits an autosomal recessive pattern of inheritance. Besides ichthyosis, systemic manifestations may be present. ...This case emphasizes the need for peripheral blood smear sc …
Dorfman-Chanarin syndrome (DCS) is a very rare disorder of lipid metabolism that exhibits an autosomal recessive pattern of in …