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4. Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness. Sevior KB; Hatamochi A; Stewart IA; Bykhovskaya Y; Allen-Powell DR; Fischel-Ghodsian N; Maw MA Am J Med Genet; 1998 Jan; 75(2):179-85. PubMed ID: 9450881 [TBL] [Abstract][Full Text] [Related]
5. [Keratosis palmoplantaris with periodontopathy (Papillon-Lefèvre syndrome) and inner ear deafness]. Hübner U; Menzel V Dermatol Monatsschr; 1988; 174(5):267-71. PubMed ID: 2969833 [No Abstract] [Full Text] [Related]
6. Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations. Sharland M; Bleach NR; Goberdhan PD; Patton MA J Med Genet; 1992 Jan; 29(1):50-2. PubMed ID: 1532426 [TBL] [Abstract][Full Text] [Related]
7. Palmoplantar keratoderma with deafness due to GJB2 mutation can develop ichthyosiform symptoms: a case report. Kimura A; Miyauchi T; Peh JT; Yanagi T; Hasegawa S; Morita S; Ujiie H J Eur Acad Dermatol Venereol; 2022 Sep; 36(9):e693-e695. PubMed ID: 35398937 [No Abstract] [Full Text] [Related]
8. Identification of a recurrent mitochondrial mutation in a Japanese family with palmoplantar keratoderma, nail dystrophy, and deafness. Hayashi R; Fujiwara H; Morishita M; Ito M; Shimomura Y Eur J Dermatol; 2015; 25(1):79-81. PubMed ID: 25513986 [No Abstract] [Full Text] [Related]
9. SERPINB7 novel mutation in Chinese patients with Nagashima-type palmoplantar keratosis and cases associated with atopic dermatitis. Zhao J; Yang Z; Xiang X; Ma L Int J Dermatol; 2020 Sep; 59(9):e320-e322. PubMed ID: 32406097 [No Abstract] [Full Text] [Related]
10. Familial hereditary, progressive sensori-neural hearing loss with keratosis palmaris and plantaris. Bititci OO J Laryngol Otol; 1975 Nov; 89(11):1143-6. PubMed ID: 127819 [No Abstract] [Full Text] [Related]
11. [Papulo-verrucoid keratodermia of the Brauer, Buschke-Fischer type]. Fernández Vozmediano JM; Lasanta Villar J Med Cutan Ibero Lat Am; 1983; 11(2):125-8. PubMed ID: 6224990 [No Abstract] [Full Text] [Related]
12. Inherited palmoplantar keratoderma and sensorineural deafness associated with A7445G point mutation in the mitochondrial genome. Martin L; Toutain A; Guillen C; Haftek M; Machet MC; Toledano C; Arbeille B; Lorette G; Rötig A; Vaillant L Br J Dermatol; 2000 Oct; 143(4):876-83. PubMed ID: 11069477 [TBL] [Abstract][Full Text] [Related]
18. Case of palmoplantar keratoderma with sensorineural deafness and mental retardation that may be another variant of syndromic palmoplantar keratoderma. Utsumi D; Hanashiro F; Miyagi T; Yamamoto Y; Uezato H; Takahashi K J Dermatol; 2013 Jul; 40(7):579-80. PubMed ID: 23594229 [No Abstract] [Full Text] [Related]
19. [Hereditary palmoplantar keratoderma - a focus on clinical and molecular genetic aspects]. Kamaleswaran S; Ousager LB; Bach RO; Bygum A Ugeskr Laeger; 2014 Feb; 176(7A):V05130280. PubMed ID: 25347558 [TBL] [Abstract][Full Text] [Related]
20. Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant trait. Tolmie JL; Wilcox DE; McWilliam R; Assindi A; Stephenson JB J Med Genet; 1988 Nov; 25(11):754-7. PubMed ID: 2976839 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]