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

Year Number of Results
1965 1
1970 1
1972 1
1973 1
1979 1
1980 1
1981 1
1983 1
1986 1
1987 1
1988 2
1989 3
1990 2
1991 1
1992 3
1993 2
1995 2
1996 3
1997 5
1999 2
2000 2
2001 7
2002 6
2003 4
2004 3
2005 4
2006 9
2007 5
2008 6
2009 3
2010 5
2011 1
2012 4
2013 4
2014 6
2015 2
2016 8
2017 6
2018 2
2019 1
2020 3
2021 7
2023 0

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122 results

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Page 1
Skin Cancer Associated Genodermatoses: A Literature Review.
Schierbeck J, Vestergaard T, Bygum A. Schierbeck J, et al. Acta Derm Venereol. 2019 Apr 1;99(4):360-369. doi: 10.2340/00015555-3123. Acta Derm Venereol. 2019. PMID: 30653245 Free article. Review.
The most common syndromes associated with basal cell carcinoma are: Gorlin-Goltz syndrome, Rombo syndrome, and Bazex-Dupre-Christol syndrome. Multiple squamous cell carcinomas can be related to: xeroderma pigmentosum, Ferguson-Smith, Muir-Torre syndrome …
The most common syndromes associated with basal cell carcinoma are: Gorlin-Goltz syndrome, Rombo syndrome, and Bazex-Dupre-Chr …
Rothmund-Thomson syndrome.
Larizza L, Roversi G, Volpi L. Larizza L, et al. Orphanet J Rare Dis. 2010 Jan 29;5:2. doi: 10.1186/1750-1172-5-2. Orphanet J Rare Dis. 2010. PMID: 20113479 Free PMC article. Review.
Rothmund-Thomson syndrome (RTS) is a genodermatosis presenting with a characteristic facial rash (poikiloderma) associated with short stature, sparse scalp hair, sparse or absent eyelashes and/or eyebrows, juvenile cataracts, skeletal abnormalities, radial ra …
Rothmund-Thomson syndrome (RTS) is a genodermatosis presenting with a characteristic facial rash (poikiloderma) associa …
Rothmund-Thomson syndrome.
Vennos EM, James WD. Vennos EM, et al. Dermatol Clin. 1995 Jan;13(1):143-50. Dermatol Clin. 1995. PMID: 7712640 Review.
Rothmund-Thomson syndrome is a rare inherited disorder characterized by poikilodermatous skin changes that appear in infancy. ...This article describes aspects of the inheritance, the incidence of characteristic features, and the malignant potential of Rot …
Rothmund-Thomson syndrome is a rare inherited disorder characterized by poikilodermatous skin changes that appear in in …
Bloom syndrome.
Arora H, Chacon AH, Choudhary S, McLeod MP, Meshkov L, Nouri K, Izakovic J. Arora H, et al. Int J Dermatol. 2014 Jul;53(7):798-802. doi: 10.1111/ijd.12408. Epub 2014 Mar 6. Int J Dermatol. 2014. PMID: 24602044 Review.
Bloom Syndrome (BS, MIM #210900) is an autosomal recessive genetic disorder caused by a mutation in the BLM gene, which codes for the DNA repair enzyme RecQL3 helicase. ...Therefore, distinguishing between BS and other dermatologic syndromes of similar presentation such as …
Bloom Syndrome (BS, MIM #210900) is an autosomal recessive genetic disorder caused by a mutation in the BLM gene, which codes for the …
Aging in Rothmund-Thomson syndrome and related RECQL4 genetic disorders.
Lu L, Jin W, Wang LL. Lu L, et al. Ageing Res Rev. 2017 Jan;33:30-35. doi: 10.1016/j.arr.2016.06.002. Epub 2016 Jun 7. Ageing Res Rev. 2017. PMID: 27287744 Review.
Rothmund-Thomson Syndrome (RTS) is a rare autosomal recessive disease which manifests several clinical features of accelerated aging. ...
Rothmund-Thomson Syndrome (RTS) is a rare autosomal recessive disease which manifests several clinical features of acce …
RECQ DNA Helicases and Osteosarcoma.
Lu L, Jin W, Wang LL. Lu L, et al. Adv Exp Med Biol. 2020;1258:37-54. doi: 10.1007/978-3-030-43085-6_3. Adv Exp Med Biol. 2020. PMID: 32767233 Review.
Humans possess five RECQ helicase genes, and mutations in three of them - BLM, WRN, and RECQL4 - are associated with the genetic disorders Bloom syndrome, Werner syndrome, and Rothmund-Thomson syndrome (RTS), respectively. ...
Humans possess five RECQ helicase genes, and mutations in three of them - BLM, WRN, and RECQL4 - are associated with the genetic disorders B …
Inherited skin disorders presenting with poikiloderma.
Rayinda T, van Steensel M, Danarti R. Rayinda T, et al. Int J Dermatol. 2021 Nov;60(11):1343-1353. doi: 10.1111/ijd.15498. Epub 2021 Mar 19. Int J Dermatol. 2021. PMID: 33739439 Review.
It is often mistaken for mottled pigmentation by general practitioners or nondermatology specialists. Poikiloderma can be a key presenting symptom of Rothmund-Thomson syndrome (RTS), dyskeratosis congenita (DC), hereditary sclerosing poikiloderma (HSP), hered …
It is often mistaken for mottled pigmentation by general practitioners or nondermatology specialists. Poikiloderma can be a key presenting s …
Kindler syndrome.
Ashton GH. Ashton GH. Clin Exp Dermatol. 2004 Mar;29(2):116-21. doi: 10.1111/j.1365-2230.2004.01465.x. Clin Exp Dermatol. 2004. PMID: 14987263 Review.
Kindler syndrome is a rare, autosomal recessive skin fragility disorder characterized by blistering in infancy, followed by photosensitivity and progressive poikiloderma. ...This article reviews the clinical features as well as the molecular and cellular pathology of Kindl …
Kindler syndrome is a rare, autosomal recessive skin fragility disorder characterized by blistering in infancy, followed by photosens …
Reticulate hyperpigmentation.
Schnur RE, Heymann WR. Schnur RE, et al. Semin Cutan Med Surg. 1997 Mar;16(1):72-80. doi: 10.1016/s1085-5629(97)80038-7. Semin Cutan Med Surg. 1997. PMID: 9125768 Review.
Other reticulate pigmentary disorders reviewed include the Naegeli-Franceschetti-Jadassohn syndrome, X-linked reticulate pigmentary disorder, dermatopathia pigmentosa reticularis, Dowling-Degos disease, dyschromatosis, confluent and reticulated papillomatosis of Gougerot a …
Other reticulate pigmentary disorders reviewed include the Naegeli-Franceschetti-Jadassohn syndrome, X-linked reticulate pigmentary d …
122 results