Dentin dysplasia - 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 …
Dentin Dysplasia Type II - Symptoms, Causes, Treatment | NORD
2024年3月5日 · Dentin dysplasia type II is a dental abnormality characterized by abnormal development (dysplasia) of dentin. Within the interior of a tooth is pulp – a specialized tissue that contains nerves, blood vessels and lymphatic vessels.
Dentin Dysplasia Type I - Symptoms, Causes, Treatment | NORD
2008年3月31日 · Dentin dysplasia type I is an inherited disorder characterized by atypical development of the “dentin” of a person’s teeth. Dentin makes up most of the tooth and is the bone-like material under the enamel. It serves to contain the pulp of the tooth.
Dentin dysplasia type I – A rare entity - PMC
Dentin dysplasia type I is an unusual abnormality of dentin which leads to premature exfoliation of the teeth. The treatment of children with dentin dysplasia aims in effective preventive care as because of the early loss of teeth due to shortened roots and periodontitis.
Dentin dysplasia | About the Disease | GARD
Dentin dysplasia (DD) is a rare disorder belonging to the group of hereditary dentin defects and is characterized by abnormal dentin structure and root development resulting in abnormal tooth development. It encompasses two subtypes: DD type I and DD type II.
Dentin dysplasia type I | About the Disease | GARD
Dentin dysplasia type I (DD-I) is a rare form of dentin dysplasia (DD, see this term) characterized by sharp conical short roots or rootless teeth.
Isolated dentinogenesis imperfecta and dentin dysplasia ...
Human mutations of this DSPP gene are responsible for three isolated dentinal diseases classified by Shield in 1973: type II and III dentinogenesis imperfecta and type II dentin dysplasia. Shield classification was based on clinical phenotypes observed in patient.