Witkop Tooth and Nail Syndrome and Orthodontics

Author:

Altug-Atac Ayse T.1,Iseri Haluk2

Affiliation:

1. a Assistant Professor, Department of Orthodontics, School of Dentistry, University of Ankara, Ankara, Turkey

2. b Professor and Chairman, Department of Orthodontics, School of Dentistry, University of Ankara, Ankara, Turkey

Abstract

Abstract This case report presents the orthodontic treatment of a patient with Witkop syndrome, an autosomal dominant genetic disorder characterized by the absence of several teeth and abnormalities of the nails. The patient, a 6-year 4-month-old boy, was referred to our clinic for treatment of severe overjet and openbite. Radiographic and clinical evaluations showed peg-shaped maxillary lateral incisors and the congenital absence of three mandibular incisors as well as spoon-shaped fingernails. Treatment of openbite and overjet was initiated with functional appliances, and fixed orthodontic appliances were inserted at age 10 years 3 months. The edentulous spaces are being maintained for implants that will be provided once the patient's growth is complete. Evaluations of long-term treatment results to date have indicated improvements in both facial and dental esthetics.

Publisher

The Angle Orthodontist (EH Angle Education & Research Foundation)

Subject

Orthodontics

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Witkop Syndrome;Genetic Syndromes;2023

2. Orthodontic and dentofacial orthopedic treatments in patients with ectodermal dysplasia: a systematic review;Orphanet Journal of Rare Diseases;2022-10-17

3. Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome;Pan African Medical Journal;2020

4. Syndromes Affecting Skin and Mucosa;Atlas of the Oral and Maxillofacial Surgery Clinics;2014-09

5. Ectodermal Dysplasias;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

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