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.
147 related articles for article (PubMed ID: 35543077)
1. Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss. Vona B; Schwartzbaum DA; Rodriguez AA; Lewis SS; Toosi MB; Radhakrishnan P; Bozan N; Akın R; Doosti M; Manju R; Duman D; Sineni CJ; Nampoothiri S; Karimiani EG; Houlden H; Bademci G; Tekin M; Girisha KM; Maroofian R; Douzgou S J Eur Acad Dermatol Venereol; 2022 Sep; 36(9):1606-1611. PubMed ID: 35543077 [TBL] [Abstract][Full Text] [Related]
2. De novo mutation in KITLG gene causes a variant of Familial Progressive Hyper- and Hypo-pigmentation (FPHH). Gorenjak M; Fijačko N; Bogomir Marko P; Živanović M; Potočnik U Mol Genet Genomic Med; 2021 Dec; 9(12):e1841. PubMed ID: 34716665 [TBL] [Abstract][Full Text] [Related]
3. KITLG mutations cause familial progressive hyper- and hypopigmentation. Amyere M; Vogt T; Hoo J; Brandrup F; Bygum A; Boon L; Vikkula M J Invest Dermatol; 2011 Jun; 131(6):1234-9. PubMed ID: 21368769 [TBL] [Abstract][Full Text] [Related]
4. Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation. Wang J; Li W; Zhou N; Liu J; Zhang S; Li X; Li Z; Yang Z; Sun M; Li M BMC Med Genomics; 2021 Jan; 14(1):12. PubMed ID: 33407466 [TBL] [Abstract][Full Text] [Related]
5. Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2. Zazo Seco C; Serrão de Castro L; van Nierop JW; Morín M; Jhangiani S; Verver EJ; Schraders M; Maiwald N; Wesdorp M; Venselaar H; Spruijt L; Oostrik J; Schoots J; ; van Reeuwijk J; Lelieveld SH; Huygen PL; Insenser M; Admiraal RJ; Pennings RJ; Hoefsloot LH; Arias-Vásquez A; de Ligt J; Yntema HG; Jansen JH; Muzny DM; Huls G; van Rossum MM; Lupski JR; Moreno-Pelayo MA; Kunst HP; Kremer H Am J Hum Genet; 2015 Nov; 97(5):647-60. PubMed ID: 26522471 [TBL] [Abstract][Full Text] [Related]
6. Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism. Gironi LC; Colombo E; Brusco A; Grosso E; Naretto VG; Guala A; Di Gregorio E; Zonta A; Zottarelli F; Pasini B; Savoia P Medicina (Kaunas); 2019 Jul; 55(7):. PubMed ID: 31284637 [TBL] [Abstract][Full Text] [Related]
7. Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation. Kato M; Yagami A; Tsukamoto T; Shinkai Y; Kato T; Kurahashi H J Dermatol; 2020 Jun; 47(6):669-672. PubMed ID: 32189379 [TBL] [Abstract][Full Text] [Related]
8. The genetic determination of skin pigmentation: KITLG and the KITLG/c-Kit pathway as key players in the onset of human familial pigmentary diseases. Picardo M; Cardinali G J Invest Dermatol; 2011 Jun; 131(6):1182-5. PubMed ID: 21566575 [TBL] [Abstract][Full Text] [Related]
9. A case of familial progressive hyperpigmentation with or without hypopigmentation presenting with hypopigmented striae along the lines of Blaschko. Hida T; Idogawa M; Ishikawa A; Okura M; Sasaki S; Tokino T; Uhara H J Dermatol; 2024 Sep; ():. PubMed ID: 39269165 [TBL] [Abstract][Full Text] [Related]
10. Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLG. Cuell A; Bansal N; Cole T; Kaur MR; Lee J; Loffeld A; Moss C; O'Donnell M; Takeichi T; Thind CK; McGrath JA Clin Exp Dermatol; 2015 Dec; 40(8):860-4. PubMed ID: 26179221 [TBL] [Abstract][Full Text] [Related]
11. Biology of human melanocyte development, Piebaldism, and Waardenburg syndrome. Saleem MD Pediatr Dermatol; 2019 Jan; 36(1):72-84. PubMed ID: 30561083 [TBL] [Abstract][Full Text] [Related]
12. Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novel KITLG mutation. Zhang J; Cheng R; Liang J; Ni C; Li M; Yao Z Br J Dermatol; 2016 Dec; 175(6):1369-1371. PubMed ID: 27106731 [No Abstract] [Full Text] [Related]
13. Waardenburg syndrome type 2 in a Turkish family: implications for the importance of the pattern of fundus pigmentation. Müllner-Eidenböck A; Moser E; Frisch H; Read AP Br J Ophthalmol; 2001 Nov; 85(11):1384-6. PubMed ID: 11702731 [No Abstract] [Full Text] [Related]
14. Waardenburg syndrome type I with heterochromia iridis and circumscribed hypopigmentation of the skin. Eigelshoven S; Kameda G; Kortüm AK; Hübsch S; Angerstein W; Singh P; Vöhringer R; Goecke T; Mayatepek E; Ruzicka T; Wildhardt G; Meissner T; Kruse R Pediatr Dermatol; 2009; 26(6):759-61. PubMed ID: 20199465 [TBL] [Abstract][Full Text] [Related]
15. Familial progressive hyper- and hypopigmentation caused by a novel mutation in site II of the KITLG gene. Liu Z; Zhu Z; Luo J; Yang B J Dermatol; 2021 Sep; 48(9):e462-e463. PubMed ID: 34114687 [No Abstract] [Full Text] [Related]
16. Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity. Xiao-Kai F; Yue-Xi H; Yan-Jia L; Li-Rong C; He-Peng W; Qing S An Bras Dermatol; 2017; 92(3):329-333. PubMed ID: 29186243 [TBL] [Abstract][Full Text] [Related]
17. Biallelic variants in PAX3 cause Klein syndrome. Salah S; Meiner V; Abumayaleh A; Asafra A; Al-Sharif T; Al-Fallah O; Hasasneh B; Zlotogora J Clin Genet; 2022 Sep; 102(3):223-227. PubMed ID: 35607853 [TBL] [Abstract][Full Text] [Related]
18. [Waardenburg syndrome type I: case report]. Silva PC; Rangel P; Couto A Arq Bras Oftalmol; 2011; 74(3):209-10. PubMed ID: 21915450 [TBL] [Abstract][Full Text] [Related]