Literature DB >> 16129001

Witkop tooth and nail syndrome: a case report.

S Devadas1, B Varma, J Mungara, T Joseph, T R Saraswathi.   

Abstract

Witkop tooth and nail syndrome is an autosomal dominant ectodermal dysplasia characterized by hypodontia and nail dysplasia. Mutations in MSX-1 have been identified as being involved in the syndrome. Mandibular incisors, secondary molars and maxillary canines are the most frequently missing teeth. Tooth shape may vary, and conical and narrow crowns are common. Nail dysplasia affects finger- and toenails, and is often more severe in childhood. Nails may be spoon-shaped, rigid, slow-growing and easily broken. The clinical and radiographic features of a mother and child presenting with this rare condition are described.

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Year:  2005        PMID: 16129001     DOI: 10.1111/j.1365-263X.2005.00647.x

Source DB:  PubMed          Journal:  Int J Paediatr Dent        ISSN: 0960-7439            Impact factor:   3.455


  2 in total

1.  Surgical and prosthetic rehabilitation of siblings with Witkop tooth and nail syndrome using zygomatic implants: a familial case series of 3 patients with up to 15-year follow-up.

Authors:  Kale B McMillan; Dane C McMillan; Kevin Arce; Thomas J Salinas
Journal:  Oral Maxillofac Surg       Date:  2022-07-30

2.  MSX1 mutation in witkop syndrome; a case report.

Authors:  Faezeh Ghaderi; Somaye Hekmat; Reza Ghaderi; Majid Fardaei
Journal:  Iran J Med Sci       Date:  2013-06
  2 in total

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