These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
100 related articles for article (PubMed ID: 3813407)
1. [The FLOTCH syndrome. Familial occurrence of total LeukOnychia, Trichilemmal cysts and Ciliary dystrophy with dominant autosomal Heredity]. Friedel J; Heid E; Grosshans E Ann Dermatol Venereol; 1986; 113(6-7):549-53. PubMed ID: 3813407 [No Abstract] [Full Text] [Related]
2. Leukonychia totalis associated with multiple pilar cysts: report of a five-generation family: FLOTCH syndrome? Rodríguez-Lojo R; Del Pozo J; Sacristán F; Barja J; Piñeyro-Molina F; Pérez-Varela L Eur J Dermatol; 2011; 21(4):484-6. PubMed ID: 21659070 [TBL] [Abstract][Full Text] [Related]
3. FLOTCH Syndrome: A Case of Leukonychia Totalis and Multiple Pilar Cysts. Mansour M; Brothers R; Brothers R Cutis; 2023 Oct; 112(4):200-202. PubMed ID: 37988304 [TBL] [Abstract][Full Text] [Related]
4. Keratosis pilaris and hereditary koilonychia without monilethrix. Thai KE; Sinclair RD J Am Acad Dermatol; 2001 Oct; 45(4):627-9. PubMed ID: 11568761 [TBL] [Abstract][Full Text] [Related]
5. Hereditary leukonychia totalis, acanthosis-nigricans-like lesions and hair dysplasia: a new syndrome? Le Corre Y; Steff M; Croue A; Filmon R; Verret JL; Le Clech C Eur J Med Genet; 2009; 52(4):229-33. PubMed ID: 19401242 [TBL] [Abstract][Full Text] [Related]
6. Molecular genetics of hereditary hair and nail disease. van Steensel MA; van Geel M; Steijlen PM Am J Med Genet C Semin Med Genet; 2004 Nov; 131C(1):52-60. PubMed ID: 15468149 [TBL] [Abstract][Full Text] [Related]
7. [A syndrome: uncombable hair. Observation of 6 members of a family with pili canaliculi, associated with pili torti, progressive alopecia, atopic eczema and hamartomas]. Braun-Falco O; Ryckmanns F; Heilgemeir GP; Ring J Hautarzt; 1982 Jul; 33(7):366-72. PubMed ID: 7107281 [TBL] [Abstract][Full Text] [Related]
12. [Colobomatous microphthalmos with cyst and 4 P- syndrome]. Baudet D; Defawe G; Le Marec B; Picard F; Nicaise A; Urvoy M Bull Soc Ophtalmol Fr; 1984 Jan; 84(1):67-8. PubMed ID: 6529828 [No Abstract] [Full Text] [Related]
13. Pili trianguli canaliculi: uncombable hair syndrome in a family with apparent autosomal dominant inheritance. de Luna MM; Rubinson R; de Kohan ZB Pediatr Dermatol; 1985 Jul; 2(4):324-7. PubMed ID: 4011511 [TBL] [Abstract][Full Text] [Related]
14. Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A. Nagy N; Wedgeworth E; Hamada T; White JM; Hashimoto T; McGrath JA J Dermatol Sci; 2010 Jun; 58(3):220-2. PubMed ID: 20418069 [No Abstract] [Full Text] [Related]
15. Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodontia. Boulé S; Fressart V; Laux D; Mallet A; Simon F; de Groote P; Bonnet D; Klug D; Charron P Int J Cardiol; 2012 Nov; 161(1):50-2. PubMed ID: 22795705 [No Abstract] [Full Text] [Related]
16. Werner's syndrome. Duvic M; Lemak NA Dermatol Clin; 1995 Jan; 13(1):163-8. PubMed ID: 7712642 [TBL] [Abstract][Full Text] [Related]