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3. [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]
4. [Pili torti et canaliculi in ectodermal dysplasia]. Trüeb RM; Spycher MA; Schumacher F; Burg G Hautarzt; 1994 Jun; 45(6):372-7. PubMed ID: 8071068 [TBL] [Abstract][Full Text] [Related]
5. Family with "pure" hair-nail ectodermal dysplasia. Barbareschi M; Cambiaghi S; Crupi AC; Tadini G Am J Med Genet; 1997 Oct; 72(1):91-3. PubMed ID: 9295083 [TBL] [Abstract][Full Text] [Related]
6. Journey toward unraveling the molecular basis of hereditary hair disorders. Shimomura Y J Dermatol Sci; 2016 Dec; 84(3):232-238. PubMed ID: 27523806 [TBL] [Abstract][Full Text] [Related]
8. Genetic hair and nail disorders. Sprecher E Clin Dermatol; 2005; 23(1):47-55. PubMed ID: 15708289 [TBL] [Abstract][Full Text] [Related]
9. [What is new in genetically-induced hair diseases?]. Traupe H; Hamm H Z Hautkr; 1990 Dec; 65(12):1085-91. PubMed ID: 2087835 [TBL] [Abstract][Full Text] [Related]
10. Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias. Itin PH; Pittelkow MR J Am Acad Dermatol; 1990 May; 22(5 Pt 1):705-17. PubMed ID: 2189905 [TBL] [Abstract][Full Text] [Related]
11. Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation. Rasool M; Nawaz S; Azhar A; Wajid M; Westermark P; Baig SM; Klar J; Dahl N Eur J Dermatol; 2010; 20(4):443-6. PubMed ID: 20409997 [TBL] [Abstract][Full Text] [Related]
12. Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia. Rossi A; Miraglia E; Fortuna MC; Calvieri S; Giustini S J Eur Acad Dermatol Venereol; 2017 Feb; 31(2):367-370. PubMed ID: 27504742 [TBL] [Abstract][Full Text] [Related]
13. Congenital atrichia and hypotrichosis. Bennàssar A; Ferrando J; Grimalt R World J Pediatr; 2011 May; 7(2):111-7. PubMed ID: 21574026 [TBL] [Abstract][Full Text] [Related]
14. Alopecia in genetic diseases. Calvieri S; Rossi A G Ital Dermatol Venereol; 2014 Feb; 149(1):1-13. PubMed ID: 24566562 [TBL] [Abstract][Full Text] [Related]
15. A form of ectodermal dysplasia; hypotrichosis with anhidrosis and anodontia. VERGER P; BENTEGEAT J; PAILLOU L J Med Bord; 1952 Oct; 129(10):868-78. PubMed ID: 13023176 [No Abstract] [Full Text] [Related]
17. Hair-nail dysplasia--a new pure autosomal dominant ectodermal dysplasia. Pinheiro M; Freire-Maia N Clin Genet; 1992 Jun; 41(6):296-8. PubMed ID: 1623625 [TBL] [Abstract][Full Text] [Related]
18. Update of recent findings in genetic hair disorders. Hayashi R; Shimomura Y J Dermatol; 2022 Jan; 49(1):55-67. PubMed ID: 34676598 [TBL] [Abstract][Full Text] [Related]
19. [Tooth and oral mucosa hereditary anomalies in complex syndromes characterized by hyper- or hypotrichosis]. Giannetti L; Consolo U; Bambini F Minerva Stomatol; 2003; 52(1-2):25-30. PubMed ID: 12686911 [TBL] [Abstract][Full Text] [Related]
20. A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type. Naeem M; Wajid M; Lee K; Leal SM; Ahmad W J Med Genet; 2006 Mar; 43(3):274-9. PubMed ID: 16525032 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]