dysplasia$23529$ - significado y definición. Qué es dysplasia$23529$
Diclib.com
Diccionario ChatGPT
Ingrese una palabra o frase en cualquier idioma 👆
Idioma:

Traducción y análisis de palabras por inteligencia artificial ChatGPT

En esta página puede obtener un análisis detallado de una palabra o frase, producido utilizando la mejor tecnología de inteligencia artificial hasta la fecha:

  • cómo se usa la palabra
  • frecuencia de uso
  • se utiliza con más frecuencia en el habla oral o escrita
  • opciones de traducción
  • ejemplos de uso (varias frases con traducción)
  • etimología

Qué (quién) es dysplasia$23529$ - definición

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         
  • An [[autosomal dominant]] pattern
  • The setup for BPAP using a mechanical ventilator
  • Cobb angle measurement of a dextroscoliosis
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.

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.