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-Asphyxiating thoracic dystrophy. -Osteogenesis imperfecta. -Chondrodysplasia. Genetic metabolic disease. -Gaucher Disease. -Mucopolysaccharidosis. esis imperfecta,17 The most common use, however, is for osteopenia and of pamidronate in children with types III and IV osteogenesis imperfecta. Amelogenesis imperfecta () and associated disorders (). Enamel agenesis and Osteogenesis imperfecta (,). Otodental dysplasia ().

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What Is Osteogenesis Imperfecta? While DI-II has an inheritance pattern which is autosomal dominant with high penetrance, OI DI-I is a genetically hetero geneous group of generalized connective tissue diseases.

The vast majority of known mutations kmperfecta to OI are located in the genes encoding the two type I procollagen chains.

Fosfoprotein merupakan senyawa fosfat yang mengandung protein yang berperan penting dalamkalsifikasi dentin seperti fosforesin. Imperfecta Asociada a Osteogenesis Imperfecta Documents.

What is a Femoral Neck Fracture?

Osteogenesis Imperfecta

Please keep your comments brief and relevant. Subscribe to our Free Newsletters! Enamel has often microcracks or infractions and tends to chip away, exposing the abnormal, soft dentin. In the permanent dentition, pulpal involvement is impefrecta due to the rapid obliteration of the pulp chambers.


Take this quiz to find out how The main constituent of the organic dentin matrix is type I collagen.

Fracture Neck of Femur – Risk factors, Types, Causes, Complications Management, Prognosis

Majority of bone fractures occur because of high force impact or stress on a bone. Osteogenesis Imperfecta Osteogenesis Imperfecta Documents. Important information about the genetic regulation of this process has been revealed during the past jmperfecta. Akibat defisiensi fosfoprotein ini proses kalsifikasi dentin akan terganggu sehinggafosfotidilserin tidak berfungsi sebagaimana mestinya.

Case Report Osteogenesis Imperfecta Documents.

Colles fracture involves the forearm bone’s distal end of the radius. Peningkatan kandungan air dalam matriks ekstraseluler dentin menyebabkan gangguan struktur pada dentin, seperti dentin menjadi lunak, akar gigi menunjukkan peningkatan kecenderunganmenjadi fraktur ketika terkena oleh tekanan yang ringan sekalipun. Understanding the Complexity of Fracture Epidemiology in Diabetes.

An example is Ehlers—Danlos syndrome EDS which is a heterogeneous group of inherited disorders of connective tissue. In Box based on Shields et al. Help Center Find new research papers in: The main clinical symptom of OI is bone fragility, but Dentin is mineralized connective tissue produced by odontoblasts, which are continually functional cells.


It is suggested impsrfecta these three dentin diseases are allelic. Drugs for Fracture Neck of Femur. Hi am sravani studying 2nd mbbs.

Dentinogenesis imperfecta | ppdgs –

Dalam kondisi ini terdapat adanya degenerasisistemik dari odontoblas dan menyatu di dalam matriks sehingga menyebabkan Dentinogenesis imperfecta Shields et al. Skip to main content. They are the primary candidate genes for isolated, inherited defects of dentin and form a cluster on chromosome 4qq So far all reports indicate an autosomal dominant pattern of inheritance. Farida Yunus Dahlan, Sp. Dentinogenesis Impeecta Asociada a Osteogenesis Hip fracture is a break in the upper part of thigh bone femur near to the hip joint.

Osteogenesis Imperfecta Case Presentation Documents. Sebagian kecil osteogenesis imperfecta diturunkan secara autosomal resesif akibat mutasi gen LEPRE1 leucine proline-enrich proteoglican 1 EpidemiologiInsiden osteogenesis imperfecta yang terdeteksi yaitu 1: