Add to ORKGTooth and Nail Syndrome or Nail Dysplasias with Hypodontiaor Witkop´s Syndrome is an autosomal dominant condition present at birth and improves by age. An early diagnosis is essential to avoid future functional, aesthetic, and psychological problems. Here we report two classic cases with brief clinical, radiological and genetic investigation along with a brief review of literature
Papillon–Lefevre syndrome (PLS) is a extreme rare of autosomal recessive inheritance characterized b...
Tooth agenesis is one of the most common craniofacial disorders in humans. More than 350 genes have ...
AbstractPapillon–Lefevre syndrome (PLS) is a very rare, autosomal recessive syndrome characterized b...
Witkop syndrome, also known as tooth and nail syndrome (TNS), is a rare autosomal dominant disorder....
Witkop′s tooth and nail syndrome is a rare autosomal dominant disorder of ectodermal dysplasi...
Summary: Tooth agenesis in the reduction of tooth number which includes hypodontia, oligodontia and ...
Objective Tooth agenesis is one of the most common craniofacial developmental anomalies. In hypodont...
Tooth agenesis constitutes one of the most common developmental anomalies in man. Oligodontia is def...
AbstractPapillon–Lefevre syndrome (PLS) is an autosomal recessive genetic disorder characterized by ...
Tooth agenesis in the reduction of tooth number which includes hypodontia, oligodontia and anodonti...
Premature tooth loss is a disastrous situation may impact on deciduous or permanent teeth era with d...
Objectives: In the present study, it is described the phenotypical analysis and the mutational scree...
Tricho-dento-osseous syndrome (TDO), an uncommon form of ectodermal dysplasia is an autosomal domina...
Demyelinating forms of Charcot-Marie-Tooth (CMT) result from mutations in a number of genes, the maj...
Objective: To understand the role of MSX1 gene in Pakistani families with hypodontia. Study Desig...
Papillon–Lefevre syndrome (PLS) is a extreme rare of autosomal recessive inheritance characterized b...
Tooth agenesis is one of the most common craniofacial disorders in humans. More than 350 genes have ...
AbstractPapillon–Lefevre syndrome (PLS) is a very rare, autosomal recessive syndrome characterized b...
Witkop syndrome, also known as tooth and nail syndrome (TNS), is a rare autosomal dominant disorder....
Witkop′s tooth and nail syndrome is a rare autosomal dominant disorder of ectodermal dysplasi...
Summary: Tooth agenesis in the reduction of tooth number which includes hypodontia, oligodontia and ...
Objective Tooth agenesis is one of the most common craniofacial developmental anomalies. In hypodont...
Tooth agenesis constitutes one of the most common developmental anomalies in man. Oligodontia is def...
AbstractPapillon–Lefevre syndrome (PLS) is an autosomal recessive genetic disorder characterized by ...
Tooth agenesis in the reduction of tooth number which includes hypodontia, oligodontia and anodonti...
Premature tooth loss is a disastrous situation may impact on deciduous or permanent teeth era with d...
Objectives: In the present study, it is described the phenotypical analysis and the mutational scree...
Tricho-dento-osseous syndrome (TDO), an uncommon form of ectodermal dysplasia is an autosomal domina...
Demyelinating forms of Charcot-Marie-Tooth (CMT) result from mutations in a number of genes, the maj...
Objective: To understand the role of MSX1 gene in Pakistani families with hypodontia. Study Desig...
Papillon–Lefevre syndrome (PLS) is a extreme rare of autosomal recessive inheritance characterized b...
Tooth agenesis is one of the most common craniofacial disorders in humans. More than 350 genes have ...
AbstractPapillon–Lefevre syndrome (PLS) is a very rare, autosomal recessive syndrome characterized b...