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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1961 1
1969 1
1971 1
1975 1
1977 1
1978 1
1980 1
1981 2
1982 1
1983 1
1984 2
1985 3
1986 1
1987 2
1988 1
1989 1
1990 4
1991 2
1992 1
1993 4
1994 2
1995 2
1996 2
1997 2
1998 1
1999 2
2000 4
2002 3
2003 2
2004 4
2005 3
2007 5
2008 4
2009 4
2010 3
2011 8
2012 4
2013 5
2014 7
2015 5
2016 4
2017 5
2018 4
2019 4
2020 3
2021 4
2022 8
2023 9
2024 3

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129 results

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Page 1
Keratosis pilaris: an update and approach to management.
Kodali N, Patel VM, Schwartz RA. Kodali N, et al. Ital J Dermatol Venerol. 2023 Jun;158(3):217-223. doi: 10.23736/S2784-8671.23.07594-1. Epub 2023 May 11. Ital J Dermatol Venerol. 2023. PMID: 37166753 Free article. Review.
We provide an updated review on the pathogenesis, clinical manifestations, and management of this common, and often annoying, finding. KP represents a family of follicular disorders, of which KP simplex is by far the most common. ...Inherited mutations of the FLG gene and …
We provide an updated review on the pathogenesis, clinical manifestations, and management of this common, and often annoying, finding. KP re …
Follicular ichthyosis.
Hazell M, Marks R. Hazell M, et al. Br J Dermatol. 1984 Jul;111(1):101-9. doi: 10.1111/j.1365-2133.1984.tb04023.x. Br J Dermatol. 1984. PMID: 6743535
We describe four patients with congenital follicular hyperkeratosis, of whom three also had pseudoacanthosis nigricans and two had facial abnormalities. ...The condition appears to constitute a distinctive form of ichthyosis in which the abnormal epidermal different …
We describe four patients with congenital follicular hyperkeratosis, of whom three also had pseudoacanthosis nigricans and two had fa …
Keratosis Pilaris.
Pennycook KB, McCready TA. Pennycook KB, et al. 2023 Jun 26. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Jun 26. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 31536314 Free Books & Documents.
Keratosis pilaris is among the most common dermatologic conditions and can be considered a normal variant. It is the most common follicular keratosis. The condition is multifactorial and innocuous, affecting the extensor surfaces of the proximal extremities. ...Keratosis p …
Keratosis pilaris is among the most common dermatologic conditions and can be considered a normal variant. It is the most common follicul …
Congenital ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis: a new genodermatosis?
Lestringant GG, Küster W, Frossard PM, Happle R. Lestringant GG, et al. Am J Med Genet. 1998 Jan 13;75(2):186-9. doi: 10.1002/(sici)1096-8628(19980113)75:2<186::aid-ajmg12>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9450882
Electron microscopic studies of ichthyotic skin did not show any specific abnormality. The association of congenital diffuse ichthyosis with follicular atrophoderma and hypotrichosis has not been reported before. The patients were reminiscent of Bazex syndrome; howe …
Electron microscopic studies of ichthyotic skin did not show any specific abnormality. The association of congenital diffuse ichthyosis …
Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processing.
Alef T, Torres S, Hausser I, Metze D, Türsen U, Lestringant GG, Hennies HC. Alef T, et al. J Invest Dermatol. 2009 Apr;129(4):862-9. doi: 10.1038/jid.2008.311. Epub 2008 Oct 9. J Invest Dermatol. 2009. PMID: 18843291 Free article.
Congenital ichthyosis encompasses a heterogeneous group of disorders of cornification. Isolated forms and syndromic ichthyosis can be differentiated. We have analyzed two consanguineous families from the United Arab Emirates and Turkey with an autosomal recessive sy …
Congenital ichthyosis encompasses a heterogeneous group of disorders of cornification. Isolated forms and syndromic ichthyosis …
Keratitis-ichthyosis-deafness syndrome and hidradenitis suppurativa.
Travis L, Ou Yang J, Andersen RK, Skovby F, Jemec GBE, Saunte DM. Travis L, et al. JAAD Case Rep. 2023 Jun 15;38:158-162. doi: 10.1016/j.jdcr.2023.06.003. eCollection 2023 Aug. JAAD Case Rep. 2023. PMID: 37555193 Free PMC article. No abstract available.
Ichthyosis follicularis syndromes in patients with mutations in GJB2.
Youssefian L, Naji M, Park JS, Rajabi F, Abdollahimajd F, Mahmoudi H, Kamyab-Hesari K, Ghalamkarpour F, Zabihi M, Teimoorian M, Youssefian L, Zeinali S, Vahidnezhad H, Uitto J. Youssefian L, et al. Clin Exp Dermatol. 2022 Aug;47(8):1561-1566. doi: 10.1111/ced.15217. Epub 2022 Jun 23. Clin Exp Dermatol. 2022. PMID: 35396755
Ichthyosis follicularis (IF) manifests as generalized spiny follicular projections found in syndromic diseases secondary to SREBF1 and MBTPS2 mutations. We sought the genetic cause of IF in two distinct families from a cohort of 180 patients with ichthyosis. …
Ichthyosis follicularis (IF) manifests as generalized spiny follicular projections found in syndromic diseases secondary to SR …
Keratitis-ichthyosis-deafness (KID) syndrome.
Gonzalez ME, Tlougan BE, Price HN, Patel R, Kamino H, Schaffer JV. Gonzalez ME, et al. Dermatol Online J. 2009 Aug 15;15(8):11. Dermatol Online J. 2009. PMID: 19891919 Free article.
These skin findings were accompanied by sensorineural hearing loss and keratoconjunctivitis, a clinical triad diagnostic of keratitis-ichthyosis-deafness (KID) syndrome. The patient also had a history of recurrent infections and cysts on the scalp. This report draws attent …
These skin findings were accompanied by sensorineural hearing loss and keratoconjunctivitis, a clinical triad diagnostic of keratitis-ich …
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome.
Mégarbané H, Mégarbané A. Mégarbané H, et al. Orphanet J Rare Dis. 2011 May 21;6:29. doi: 10.1186/1750-1172-6-29. Orphanet J Rare Dis. 2011. PMID: 21600032 Free PMC article. Review.
The IFAP syndrome is a rare X-linked genetic disorder reported in nearly 40 patients. It is characterized by the triad of Ichthyosis Follicularis, Alopecia, and Photophobia from birth. Other features such as short stature, intellectual disability, and seizures may develop …
The IFAP syndrome is a rare X-linked genetic disorder reported in nearly 40 patients. It is characterized by the triad of Ichthyosis …
129 results