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Witkop sendromu (diş-tırnak sendromu; ectodermal dysplasia 3)

Kalıtsal - AD

Ektodermal displazi bulguları (hafif)

Mikrodonti

Taurodontism

Hipodonti

Dişlerde sürme aksamaları

Tırnaklar yapı ve biçim bozuklukları

Saçlar ince/normal

Bkz Ektodermal displaziler

  • Jumlongras D, Bei M, Stimson JM, et al. A nonsense mutation in MSX1 causes Witkop syndrome. American Journal of Human Genetics, 69: 67-74, 2001

  • Wicomb GM, Stephen LX, Beighton P. Dental implications of Tooth-Nail dysplasia (Witkop syndrome): a report of an affected family and an approach to dental management. The Journal of Clinical Pediatric Dentistry, 28(2):107-112, 2004

  • Devadas S, Varma B, Mungara J, et al. Witkop tooth and nail syndrome: a case report. International Journal of Paediatric Dentistry, 15(5):364-369, 2005

  • Subramaniam P, Neeraja G. Witkop's tooth and nail syndrome: a multifaceted approach to dental management. Journal of Indian Society of Pedodontics and Preventive Dentistry, 26(1):22-25, 2008

  • Priolo M. Ectodermal dysplasias: An overview and update of clinical and molecular-functional mechanisms. American Journal of Medical Genetics, 149A:2003–2013, 2009

  • Visinoni AF, Lisboa-Costa T, Pagnan NAB, Chautard-Freire-Maia EA. Ectodermal dysplasias: Clinical and molecular review. American Journal of Medical Genetics, 149A:1980–2002, 2009

  • Ceyhan D, Kırzıoğlu Z, Calapoğlu NS. Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies. Indian Journal of Dentistry, 5(4):172-182, 2014