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Inserisci una parola o una frase in qualsiasi lingua 👆

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Traduzione e analisi delle parole tramite l'intelligenza artificiale ChatGPT

In questa pagina puoi ottenere un'analisi dettagliata di una parola o frase, prodotta utilizzando la migliore tecnologia di intelligenza artificiale fino ad oggi:

come viene usata la parola
frequenza di utilizzo
è usato più spesso nel discorso orale o scritto
opzioni di traduzione delle parole
esempi di utilizzo (varie frasi con traduzione)
etimologia

Cosa (chi) è dysplasia linguofacialis - definizione

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.

https://en.wikipedia.org/wiki/Dentin_dysplasia

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.

https://en.wikipedia.org/wiki/Campomelic_dysplasia

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.

https://en.wikipedia.org/wiki/Kniest_dysplasia

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.

https://en.wikipedia.org/wiki/Dentin dysplasia