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3. Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome). Steiner CE; Cintra ML; Marques-de-Faria AP Am J Med Genet; 2002 Dec; 113(4):381-4. PubMed ID: 12457412 [TBL] [Abstract][Full Text] [Related]
4. Autosomal recessive ectodermal dysplasia: I. An undescribed dysplasia/malformation syndrome. Bustos T; Simosa V; Pinto-Cisternas J; Abramovits W; Jolay L; Rodriguez L; Fernandez L; Ramela M Am J Med Genet; 1991 Dec; 41(4):398-404. PubMed ID: 1776626 [TBL] [Abstract][Full Text] [Related]
5. Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features. Anton-Lamprecht I; Schleiermacher E; Wolf M Birth Defects Orig Artic Ser; 1988; 24(2):183-95. PubMed ID: 3179426 [No Abstract] [Full Text] [Related]
6. Focal palmoplantar and gingival keratosis: a distinct palmoplantar ectodermal dysplasia with epidermolytic alterations but lack of mutations in known keratins. Kolde G; Hennies HC; Bethke G; Reichart PA J Am Acad Dermatol; 2005 Mar; 52(3 Pt 1):403-9. PubMed ID: 15761417 [TBL] [Abstract][Full Text] [Related]
7. Bazex-Dupré-Christol syndrome: an ectodermal dysplasia with skin appendage neoplasms. Castori M; Castiglia D; Passarelli F; Paradisi M Eur J Med Genet; 2009; 52(4):250-5. PubMed ID: 19138767 [TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive hypohidrotic ectodermal dysplasia with subclinical manifestation in the heterozygote. Passarge E; Fries E Birth Defects Orig Artic Ser; 1977; 13(3C):95-100. PubMed ID: 890117 [TBL] [Abstract][Full Text] [Related]
14. Trichoodontoonychial dysplasia--a new meso-ectodermal dysplasia. Pinheiro M; Freire-Maia N; Roth AJ Am J Med Genet; 1983 May; 15(1):67-70. PubMed ID: 6859125 [TBL] [Abstract][Full Text] [Related]
15. Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome. Rodini ES; Richieri-Costa A Am J Med Genet; 1990 Aug; 36(4):473-6. PubMed ID: 2167611 [TBL] [Abstract][Full Text] [Related]
16. Schöpf-Schulz-Passarge syndrome with an unusual pattern of inheritance. Craigen WJ; Levy ML; Lewis RA Am J Med Genet; 1997 Aug; 71(2):186-8. PubMed ID: 9217219 [TBL] [Abstract][Full Text] [Related]
17. [Familial congenital hypotrichosis with "uncombable hair," retinal pigmentary dystrophy, juvenile cataract and brachymetacarpia: another entity of the ectodermal dysplasia group]. Bork K; Stender E; Schmidt D; Berzas C; Rochels R Hautarzt; 1987 Jun; 38(6):342-7. PubMed ID: 3654205 [TBL] [Abstract][Full Text] [Related]
18. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia. Fadhil M; Ghabra TA; Deeb M; Der Kaloustian VM Am J Med Genet; 1983 Feb; 14(2):335-46. PubMed ID: 6837628 [TBL] [Abstract][Full Text] [Related]
19. Cataracts, alopecia, and sclerodactyly: a previously apparently undescribed ectodermal dysplasia syndrome on the island of Rodrigues. Wallis C; Ip FS; Beighton P Am J Med Genet; 1989 Apr; 32(4):500-3. PubMed ID: 2773993 [TBL] [Abstract][Full Text] [Related]
20. A Novel Homozygous Missense Mutation in HOXC13 Leads to Autosomal Recessive Pure Hair and Nail Ectodermal Dysplasia. Li X; Orseth ML; Smith JM; Brehm MA; Agim NG; Glass DA Pediatr Dermatol; 2017 Mar; 34(2):172-175. PubMed ID: 28297138 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]