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Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, 2017
Dentin dysplasia (DD) is a rare developmental dentin disorder that causes root malformation. It is divided into radicular DD type 1 (DD-1) and coronal DD type 2 (DD-2). Recently, a new entity causing localized root malformation of permanent first molars that resembles DD-1b has been described as molar-incisor malformation (MIM). We report and compare 4
Hiba, Qari +3 more
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Dentin dysplasia (DD) is a rare developmental dentin disorder that causes root malformation. It is divided into radicular DD type 1 (DD-1) and coronal DD type 2 (DD-2). Recently, a new entity causing localized root malformation of permanent first molars that resembles DD-1b has been described as molar-incisor malformation (MIM). We report and compare 4
Hiba, Qari +3 more
openaire +2 more sources
Radicular (Type I) dentin dysplasia
Oral Surgery, Oral Medicine, Oral Pathology, 1977Radicular dentin dysplasia is a peculiar anomaly in which abnormal dentin resembling the plici-dentin found in certain fish and reptiles obliterates the pulp chamber. The almost complete absence of roots leads to the early loss of teeth and predisposes to paradontal infection and the formation of cysts.
T. Perl, A.G. Farman
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The Journal of the Dental Association of Thailand, 1990
Dentinal dysplasia is one of the rarest hereditary disturbances of dentin formation characterized by the teeth present with short blunt roots, considerably reduced or obliterated pulp spaces, periapical abscess or cysts without an obvious causative factor, and spontaneous exfoliated.
D, Tongnoi, T, Triratana, S, Arunakul
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Dentinal dysplasia is one of the rarest hereditary disturbances of dentin formation characterized by the teeth present with short blunt roots, considerably reduced or obliterated pulp spaces, periapical abscess or cysts without an obvious causative factor, and spontaneous exfoliated.
D, Tongnoi, T, Triratana, S, Arunakul
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Oral Surgery, Oral Medicine, Oral Pathology, 1967
Richard P. Elzay, C.Theodore Robinson
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Richard P. Elzay, C.Theodore Robinson
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Dentin dysplasia type I: five cases within one family.
Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics, 1998Five cases of dentin dysplasia type I within one family are described. Clinically and radiologically, such patients are characterized by a delayed eruption pattern, opacity of the incisional margins, hypermobility of the teeth, short and defective roots, and obliterated pulp chambers. A conservative attitude toward the treatment of common conditions in
Kalk, WWI, Batenburg, RHK, Vissink, A
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Dentin dysplasia: single-tooth involvement?
Quintessence international (Berlin, Germany : 1985), 2009Dentin dysplasia is a genetic defect of dentin formation inherited as an autosomal dominant trait. It is characterized by normal enamel but atypical dentin formation with abnormal pulpal morphology. Once thought to be a single entity, dentin dysplasia has now been divided into type I (radicular) and II (coronal). Type I is by far the more common.
Veena V, Naik, Alka D, Kale
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Radicular (type 1) dentin dysplasia.
Oral surgery, oral medicine, and oral pathology, 1977Radicular dentin dysplasia is a peculiar anomaly in which abnormal dentin resembling the plici-dentin found in certain fish and reptiles obliterates the pulp chamber. The almost complete absence of roots leads to the early loss of teeth and predisposes to paradontal infection and the formation of cysts.
T, Perl, A G, Farman
openaire +1 more source