dysplasia hemimelica - definitie. Wat is dysplasia hemimelica
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Wat (wie) is dysplasia hemimelica - definitie

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

Trevor disease         
  • 3D CT image of Trevor's disease of the ankle and talus.
ORTHOPEDIC DISEASE
Trevor's disease; Trevors disease; Dysplasia epiphysealis hemimelica
Trevor disease, also known as dysplasia epiphysealis hemimelica and Trevor's disease, is a congenital bone developmental disorder. There is 1 case per million population.
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.

Wikipedia

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.