The muscle segment homeobox (MSX1) gene plays a crucial role in epithelial-mesenchymal
tissue interactions in craniofacial development. It plays a regulative role in cellular …

Objective To provide an evidence-based resource for paleopathologists to consider multiple
skeletal indicators of pathology associated with early tooth loss in children to aid in …

Tooth agenesis is one of the most common craniofacial disorders in humans. More than 350
genes have been associated with teeth development. In this study, we enrolled 60 child …

Background Tooth agenesis is a common developmental dental anomaly. The aim of the
study was to identify the causal genetic mutation in a four-generation Chinese family …

Abstract Tooth and Nail Syndrome or Nail Dysplasias with Hypodontiaor Witkops Syndrome
is an autosomal dominant condition present at birth and improves by age. An early …

ÖzetOral kavite farklı histolojik yapısı ve işlevi bulunan dokulardan oluştuğundan benign,
premalign ve malign karakterli lezyonlar ortaya çıkabilir. Malign karakterli olanlar, premalign …

Ectodermal dysplasia (ED) is a congenital heterogenic disorder caused by the defect in the
ectoderm and its derivatives. This complex disorder has different subtypes, the most …

El síndrome Witkop es un padecimiento autosómico dominante con una incidencia
estimada de 2/10,000 nacimientos, cuya afectación es exclusiva de dientes y uñas. Se …

Witkop syndrome is a rare and benign autosomal dominant illness that often goes unnoticed
due to dental and nail involvement. The clinical case of a 9-year-olf female who came to the …

Vývoj zubů (odontogeneze) je komplikovaný a dynamický proces, kterého se zúčastňuje
celá řada proteinů. Vzájemnými interakcemi mezi sebou vytváří spletitou signální síť …