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

Year Number of Results
1959 1
1961 1
1964 2
1966 1
1967 1
1968 4
1970 6
1973 2
1974 4
1975 5
1976 4
1977 10
1978 6
1979 3
1980 5
1981 8
1982 1
1983 7
1984 6
1985 6
1986 7
1987 13
1988 11
1989 18
1990 13
1991 4
1992 20
1993 15
1994 12
1995 11
1996 16
1997 15
1998 18
1999 16
2000 19
2001 22
2002 19
2003 21
2004 29
2005 30
2006 20
2007 30
2008 36
2009 48
2010 36
2011 58
2012 52
2013 62
2014 68
2015 64
2016 52
2017 52
2018 53
2019 61
2020 53
2021 47
2022 54
2023 46
2024 15

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1,191 results

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Page 1
Cleft Lip and Palate in Ectodermal Dysplasia.
Ganske IM, Irwin T, Langa O, Upton J 3rd, Tan WH, Mulliken JB. Ganske IM, et al. Cleft Palate Craniofac J. 2021 Feb;58(2):237-243. doi: 10.1177/1055665620949124. Epub 2020 Aug 30. Cleft Palate Craniofac J. 2021. PMID: 32864997
OBJECTIVE: Ectodermal dysplasia (ED) comprises multiple syndromes that affect skin, hair, nails, and teeth, and sometimes are associated with orofacial clefting. ...Anatomic categories were bilateral CL/P (67%), unilateral CL/P (8%), and cleft palate only (25%). The …
OBJECTIVE: Ectodermal dysplasia (ED) comprises multiple syndromes that affect skin, hair, nails, and teeth, and sometimes are …
Diagnosis and treatment in anhidrotic ectodermal dysplasia with immunodeficiency.
Kawai T, Nishikomori R, Heike T. Kawai T, et al. Allergol Int. 2012 Jun;61(2):207-17. doi: 10.2332/allergolint.12-RAI-0446. Allergol Int. 2012. PMID: 22635013 Free article. Review.
Anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) is characterized according to its various manifestations, which include ectodermal dysplasia, vascular anomalies, osteopetrosis, and diverse immunological abnormalities such as susceptibili …
Anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) is characterized according to its various manifestations, which …
Hypohidrotic ectodermal dysplasia: clinical and molecular review.
Reyes-Reali J, Mendoza-Ramos MI, Garrido-Guerrero E, Méndez-Catalá CF, Méndez-Cruz AR, Pozo-Molina G. Reyes-Reali J, et al. Int J Dermatol. 2018 Aug;57(8):965-972. doi: 10.1111/ijd.14048. Epub 2018 May 31. Int J Dermatol. 2018. PMID: 29855039 Review.
Hypohidrotic Ectodermal Dysplasia (HED) is a genetic human disorder which affects structures of ectodermal origin. ...
Hypohidrotic Ectodermal Dysplasia (HED) is a genetic human disorder which affects structures of ectodermal origin. ...
Clinical and Molecular Genetic Analysis of Cases with Ectodermal Dysplasia.
Yapijakis C, Douka A, Gintoni I, Agiannitopoulos K, Vlachakis D, Chrousos GP. Yapijakis C, et al. Adv Exp Med Biol. 2023;1423:181-186. doi: 10.1007/978-3-031-31978-5_15. Adv Exp Med Biol. 2023. PMID: 37525042
RESULTS: The clinical diagnosis of common X-linked recessive hypohidrotic ectodermal dysplasia (HED) was suspected in five male patients with partial anodontia of baby and permanent teeth, hypohidrosis, and thin hair from three families. ...A female patient had the …
RESULTS: The clinical diagnosis of common X-linked recessive hypohidrotic ectodermal dysplasia (HED) was suspected in five mal …
LEF1 haploinsufficiency causes ectodermal dysplasia.
Lévy J, Capri Y, Rachid M, Dupont C, Vermeesch JR, Devriendt K, Verloes A, Tabet AC, Bailleul-Forestier I. Lévy J, et al. Clin Genet. 2020 Apr;97(4):595-600. doi: 10.1111/cge.13714. Epub 2020 Feb 17. Clin Genet. 2020. PMID: 32022899
We report two unrelated patients with 4q25 de novo deletion encompassing LEF1, associated with severe oligodontia of primary and permanent dentition, hypotrichosis and hypohidrosis compatible with hypohidrotic ectodermal dysplasia. Taurodontism and a particular alve …
We report two unrelated patients with 4q25 de novo deletion encompassing LEF1, associated with severe oligodontia of primary and permanent d …
Ectrodactyly-Ectodermal Dysplasia-Cleft Syndrome: Ocular Findings and Surgical Treatment.
Grauhan LD, Gericke A, Brueggemann FB, Pfeiffer N, Wasielica-Poslednik J. Grauhan LD, et al. Cornea. 2023 Sep 1;42(9):1172-1175. doi: 10.1097/ICO.0000000000003295. Epub 2023 Jun 21. Cornea. 2023. PMID: 37351863
PURPOSE: Ectrodactyly-ectodermal dysplasia-cleft (EEC) syndrome is a rare genetic disorder. ...
PURPOSE: Ectrodactyly-ectodermal dysplasia-cleft (EEC) syndrome is a rare genetic disorder. ...
Aplasia cutis congenita.
Higgins C, Price A, Craig S. Higgins C, et al. BMJ Case Rep. 2022 Sep 13;15(9):e251533. doi: 10.1136/bcr-2022-251533. BMJ Case Rep. 2022. PMID: 36100287 No abstract available.
X-linked hypohidrotic ectodermal dysplasia (XLHED): clinical and diagnostic insights from an international patient registry.
Fete M, Hermann J, Behrens J, Huttner KM. Fete M, et al. Am J Med Genet A. 2014 Oct;164A(10):2437-42. doi: 10.1002/ajmg.a.36436. Epub 2014 Mar 24. Am J Med Genet A. 2014. PMID: 24664614 Review.
The web-based Ectodermal Dysplasia International Registry (EDIR) is a comprehensive patient-reported survey contributing to an understanding of ectodermal dysplasia (ED). ...
The web-based Ectodermal Dysplasia International Registry (EDIR) is a comprehensive patient-reported survey contributing to an …
Emerging therapies in genodermatoses.
Silverberg N. Silverberg N. Clin Dermatol. 2020 Jul-Aug;38(4):462-466. doi: 10.1016/j.clindermatol.2020.03.006. Epub 2020 Mar 24. Clin Dermatol. 2020. PMID: 32972604 Review.
1,191 results