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dysplasia epiphysialia punctata - translation to russian
медицина
эпифизарная точечная остеодисплазия
медицина
дентинная остеодисплазия
.jpg?width=200 "Dental abnormalities in a 5-year-old girl from north Sweden family who had various symptoms of autosomal dominant hypohidrotic ectodermal dysplasia (HED):<br>
a) Intraoral view. Note that the upper incisors have been restored with composite material to disguise their original conical shape.<br>
b) Orthopantomogram showing absence of ten primary and eleven permanent teeth in the jaws of the same individual.")
медицина
эктодермальная дисплазия
Definition
Wikipedia
Dentin dysplasia (DD) is a rare genetic developmental disorder affecting dentine production of the teeth, commonly exhibiting an autosomal dominant inheritance that causes malformation of the root. It affects both primary and permanent dentitions in approximately 1 in every 100,000 patients. It is characterized by presence of normal enamel but atypical dentin with abnormal pulpal morphology. Witkop in 1972 classified DD into two types which are Type I (DD-1) is the radicular type, and type II (DD-2) is the coronal type. DD-1 has been further divided into 4 different subtypes (DD-1a,1b,1c,1d) based on the radiographic features.
