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723 results

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Page 1
X-Linked Ichthyosis.
Crane JS, Paller AS. Crane JS, et al. 2024 Jan 25. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2024 Jan 25. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 28846233 Free Books & Documents.
X-linked ichthyosis (MIM #308100), also known as steroid sulfatase (STS) deficiency and X-linked recessive ichthyosis, is a recessive, nonsyndromic genetic skin disorder. ...With an incidence of 1 in 2500 to 1 in 6000 males, X-l …
X-linked ichthyosis (MIM #308100), also known as steroid sulfatase (STS) deficiency and X-linked recessiv …
Revisiting X-linked congenital ichthyosis.
Zhou B, Liang C, Li P, Xiao H. Zhou B, et al. Int J Dermatol. 2025 Jan;64(1):51-61. doi: 10.1111/ijd.17396. Epub 2024 Jul 31. Int J Dermatol. 2025. PMID: 39086014 Review.
X-linked recessive ichthyosis (XLI) is a hereditary skin disease characterized by generalized dryness and scaling of the skin, with frequent extracutaneous manifestations. It is the second most common type of ichthyosis, with a prevalence of 1/6,000 to …
X-linked recessive ichthyosis (XLI) is a hereditary skin disease characterized by generalized dryness and scaling of th …
X-linked ichthyosis: New insights into a multi-system disorder.
Wren GH, Davies W. Wren GH, et al. Skin Health Dis. 2022 Oct 17;2(4):e179. doi: 10.1002/ski2.179. eCollection 2022 Dec. Skin Health Dis. 2022. PMID: 36479267 Free PMC article. Review.
BACKGROUND: X-linked ichthyosis (XLI) is a rare genetic condition almostexclusively affecting males; it is characterised by abnormal desquamation and retentionhyperkeratosis, and presents with polygonal brown scales. ...
BACKGROUND: X-linked ichthyosis (XLI) is a rare genetic condition almostexclusively affecting males; it is characterise …
X-linked ichthyosis.
Shapiro LJ. Shapiro LJ. Int J Dermatol. 1981 Jan-Feb;20(1):26-31. doi: 10.1111/j.1365-4362.1981.tb05280.x. Int J Dermatol. 1981. PMID: 7009454 Review. No abstract available.
X-linked ichthyosis: an update.
Hernández-Martín A, González-Sarmiento R, De Unamuno P. Hernández-Martín A, et al. Br J Dermatol. 1999 Oct;141(4):617-27. doi: 10.1046/j.1365-2133.1999.03098.x. Br J Dermatol. 1999. PMID: 10583107 Review.
X-linked ichthyosis is a genetic disorder of keratinization characterized by a generalized desquamation of large, adherent, dark brown scales. ...Interestingly, this region escapes X chromosome inactivation and has the highest ratio of chromosomal deletions a …
X-linked ichthyosis is a genetic disorder of keratinization characterized by a generalized desquamation of large, adher …
X-linked ichthyosis: an oculocutaneous genodermatosis.
Fernandes NF, Janniger CK, Schwartz RA. Fernandes NF, et al. J Am Acad Dermatol. 2010 Mar;62(3):480-5. doi: 10.1016/j.jaad.2009.04.028. Epub 2010 Jan 18. J Am Acad Dermatol. 2010. PMID: 20080321 Review.
X-linked ichthyosis (XLI) is an X-linked recessive disorder of cutaneous keratinization with possible extracutaneous manifestations. It was first described as a distinct type of ichthyosis in 1965. XLI is caused by a deficiency in steroid …
X-linked ichthyosis (XLI) is an X-linked recessive disorder of cutaneous keratinization with possible ext …
Comorbid Medical Issues in X-Linked Ichthyosis.
Brcic L, Wren GH, Underwood JFG, Kirov G, Davies W. Brcic L, et al. JID Innov. 2022 Feb 17;2(3):100109. doi: 10.1016/j.xjidi.2022.100109. eCollection 2022 May. JID Innov. 2022. PMID: 35330591 Free PMC article. No abstract available.
Inherited ichthyosis: Non-syndromic forms.
Takeichi T, Akiyama M. Takeichi T, et al. J Dermatol. 2016 Mar;43(3):242-51. doi: 10.1111/1346-8138.13243. J Dermatol. 2016. PMID: 26945532 Review.
Non-syndromic ichthyoses include ichthyosis vulgaris, recessive X-linked ichthyosis, autosomal recessive congenital ichthyosis, keratinopathic ichthyosis and other forms. This review focuses on updates for each type of non-syndromic ic …
Non-syndromic ichthyoses include ichthyosis vulgaris, recessive X-linked ichthyosis, autosomal recessive congeni …
X-linked ichthyosis.
Das A, Mishra V. Das A, et al. Indian Pediatr. 2014 Aug;51(8):678. Indian Pediatr. 2014. PMID: 25129014 Free article. No abstract available.
Cardiac arrhythmia in individuals with steroid sulfatase deficiency (X-linked ichthyosis): candidate anatomical and biochemical pathways.
Wren GH, Davies W. Wren GH, et al. Essays Biochem. 2024 Dec 4;68(4):423-429. doi: 10.1042/EBC20230098. Essays Biochem. 2024. PMID: 38571328 Free PMC article. Review.
Recent studies have indicated that Xp22.31 genetic deletions encompassing STS (associated with the rare dermatological condition X-linked ichthyosis), and common variants within the STS gene, are associated with a markedly elevated risk of cardiac arrhythmias …
Recent studies have indicated that Xp22.31 genetic deletions encompassing STS (associated with the rare dermatological condition X- …
723 results