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Quoted phrase not found in phrase index: "Autosomal recessive congenital ichthyosis 11"
Page 1
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 …
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 …
Liver transplant in a case of arthrogryposis-renal tubular dysfunction-cholestasis syndrome with severe intractable pruritus.
Dehghani SM, Bahador A, Nikeghbalian S, Salahi H, Geramizadeh B, Malekpour A, Malek-Hosseini SA. Dehghani SM, et al. Exp Clin Transplant. 2013 Jun;11(3):290-2. doi: 10.6002/ect.2012.0202. Epub 2012 Nov 22. Exp Clin Transplant. 2013. PMID: 23190456 Free article.
Arthrogryposis-renal tubular dysfunction-cholestasis syndrome (MIM No. 208085) is a rare multisystem disorder involving the liver, kidney, skin, and central nervous and musculoskeletal systems. The syndrome is an autosomal-recessive trait, associated with germ-line …
Arthrogryposis-renal tubular dysfunction-cholestasis syndrome (MIM No. 208085) is a rare multisystem disorder involving the liver, kidney, s …
Bathing suit ichthyosis caused by a TGM1 mutation in a Tunisian child.
Benmously-Mlika R, Zaouak A, Mrad R, Laaroussi N, Abdelhak S, Hovnanian A, Mokhtar I. Benmously-Mlika R, et al. Int J Dermatol. 2014 Dec;53(12):1478-80. doi: 10.1111/ijd.12569. Epub 2014 Sep 10. Int J Dermatol. 2014. PMID: 25209454
BACKGROUND: Bathing suit ichthyosis (BSI) is an uncommon phenotype classified as a minor variant of autosomal recessive congenital ichthyosis (ARCI). ...Of these 20 missense mutations, nine occurred only in patients with the BSI phenotype and …
BACKGROUND: Bathing suit ichthyosis (BSI) is an uncommon phenotype classified as a minor variant of autosomal recessive …