Genetic and structural alterations of enamel and dentin- amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia
نویسندگان
چکیده
منابع مشابه
Dentin Dysplasia Type I with Hypomature Amelogenesis Imperfecta in an 18-year-old Girl
Introduction: Dentin dysplasia is a rare autosomal dominant inheriting disturbance of dentin formation characterized by normal enamel formation, but atypical dentin with abnormal pulpal morphology. There are two major patterns: type I and type II. Amelogenesis imperfecta is an autosomal dominant. X-link inherent disease that is classified by clinical manifestation into hypoplastic, hyp...
متن کاملEnamel protein in smooth hypoplastic amelogenesis imperfecta.
Amelogenesis imperfecta (AI) remains a poorly understood group of hereditary enamel defects characterized by a wide array of clinical presentations. Although numerous reports have described the histological features of AI, knowledge concerning the biochemical composition of the affected enamel remains minimal. The purpose of this investigation was to examine the protein of smooth hypoplastic AI...
متن کاملImmunocytochemical Detection of Dentin Matrix Proteins in Primary Teeth from Patients with Dentinogenesis Imperfecta Associated with Osteogenesis Imperfecta
Dentinogenesis imperfecta determines structural alterations of the collagen structure still not completely elucidated. Immunohistochemical analysis was used to assay Type I and VI collagen, various non-collagenous proteins distribution in human primary teeth from healthy patients or from patients affected by type I dentinogenesis imperfecta (DGI-I) associated with osteogenesis imperfecta (OI). ...
متن کاملdentin dysplasia type i with hypomature amelogenesis imperfecta in an 18-year-old girl
introduction: dentin dysplasia is a rare autosomal dominant inheriting disturbance of dentin formation characterized by normal enamel formation, but atypical dentin with abnormal pulpal morphology. there are two major patterns: type i and type ii. amelogenesis imperfecta is an autosomal dominant. x-link inherent disease that is classified by clinical manifestation into hypoplastic, hypomature, ...
متن کاملHereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia
The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal dominant genetic conditions characterised by abnormal dentine structure affecting either the primary or both the primary and secondary dentitions. DGI is reported to have an incidence of 1 in 6,000 to 1 in 8,000, whereas that of DD type 1 is 1 in 100,000. Clinically, the t...
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ژورنال
عنوان ژورنال: Journal of Dental Health, Oral Disorders & Therapy
سال: 2019
ISSN: 2373-4345
DOI: 10.15406/jdhodt.2019.10.00494