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%ما هو (من)٪ 1 - تعريف
TEETH HARD TISSUE DISEASE CHARACTERIZED BY PRESENCE OF NORMAL ENAMEL BUT ATYPICAL DENTIN WITH ABNORMAL PULPAL MORPHOLOGY
Dentinal dysplasia; Dentin dysplasia, radicular; Dentin dysplasia, coronal
Dentin dysplasia
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.
Campomelic dysplasia
OSTEOCHONDRODYSPLASIA THAT HAS MATERIAL BASIS IN A MUTATION IN CHROMOSOME 17 WHICH RESULTS IN BOWING IN THE LOCATED IN TIBIA OR LOCATED IN FEMUR
Camptomelic dysplasia
Campomelic dysplasia (CMD) is a genetic disorder characterized by bowing of the long bones and many other skeletal and extraskeletal features.Unger S, Scherer G, Superti-Furga A.
Kniest dysplasia
HUMAN DISEASE
Kniest chondrodystrophy; Kniest syndrome; Metatropic dwarfism, type II; Metatropic dysplasia type II; Swiss cheese cartilage dysplasia
Kniest dysplasia is a rare form of dwarfism caused by a mutation in the COL2A1 gene on chromosome 12. The COL2A1 gene is responsible for producing type II collagen.
ويكيبيديا
Dentin dysplasia
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.
