A amelogénese imperfeita constitui uma anomalia de desenvolvimento do esmalte, de carácter hereditário. A sua prevalência é de , podendo o esmalte. Amelogenesis imperfecta (AI) is a congenital disorder that presents with a rare abnormal formation of the enamel or external layer of the crown of teeth. 19 jul. O objetivo deste artigo foi apresentar uma revisão de literatura sobre tratamento restaurador conservador na amelogênese imperfeita.
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Thus, without a high-quality evidence, the authors planned the treatment in stages according to priority. D ICD – Besides choosing a technique, further aspects that must be taken into consideration during the design of a treatment plan are the desires and expectations of the patient or parents, the socioeconomic status, the AI type and severity, the age of the patient, the overall oral health and the cooperation of the patient for the performance of the procedures In these appointments, the conditions of the GIC restorations of the posterior teeth will be evaluated.
Condition is of autosomal dominant, autosomal recessive, or x-linked pattern.
The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Summary and related texts. For these restorations, prefabricated acetate crowns were selected.
The gene can be transmitted either as an autosomal dominant or autosomal recessive trait, or it can be X-linked. Hunter syndrome Purine—pyrimidine metabolism: Normally, the dentist should first reduce or eliminate tooth sensitivity, improve aesthetics and provide oral hygiene orientation. Disease definition Autosomal recessive brachyolmia-amelogenesis imperfecta syndrome is an exceedingly rare form of brachyolmia see this termimpefreita by mild platyspondyly, broad ilia, elongated femoral necks with coxa valga, scoliosis, and short trunked short stature associated imperteita amelogenesis imperfecta see this term of both primary and permanent dentition.
The GIC is an important material in the minimally invasive dental practice, and it stands out by its adhesion to the dental structure, linear thermal expansion coefficient similar to the tooth, biocompatibility, fluoride release, and easy technique Introduction Amelogenesis imperfecta AI is a hereditary anomaly of the enamel, which affects both dentitions and may cause tooth sensitivity, loss of vertical dimension, enamel deficiencies, pulp calcification, failed tooth eruption, impaction of permanent teeth and aesthetic commitment 12.
J Oral Maxillofac Pathol ; Enamel appears less radioopaque compared to dentine on radiographs.
Amelogenesis imperfecta – Wikipedia
No direct relation between the two conditions shown by the patient can be found in the Literature. This type of inheritance means one copy of the altered gene in each cell is sufficient to cause the disorder.
J Appl Oral Sci ; The dental care of patients im;erfeita by disabilities is often out of the usual routine, requiring specialized knowledge, greater sensitivity, increased attention and adequate environment 7. At the buccal, lingual or palatal and occlusal faces Figs. A study of the dental treatment needs of children with disabilities in Melbourne Australia.
The treatment of these cases is related to many factors, including age, damage severity, aesthetics, socioeconomic status, psychosocial aspects, and functional and social demands 1416 Phys Ther ; Through radiographs, it is possible to confirm the condition on both dentitions, which agrees with other reports on amelogenesis imperfecta However, in the posterior teeth, the patient reported pain when ingesting cold or citrus foods and sensitivity level 8 on the visual analogue scale to classify tooth sensitivity asmild, moderate or severe, after application of an air jet at a distance of 10 cm, for about 2 s.
Autosomal recessive brachyolmia-amelogenesis imperfecta syndrome is an exceedingly rare form of brachyolmia see this termcharacterized by mild platyspondyly, broad ilia, elongated femoral necks with coxa valga, scoliosis, and short trunked short stature associated with amelogenesis imperfecta see this term of both primary and permanent dentition.
The patient showed improvement in hygiene and considerable reduction of gingival inflammation. Oral manifestations include yellow and misshaped teeth, delayed tooth eruption, and intrapulpal calcifications. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. O paciente com necessidades especiais na odontologia: Moreover, the patient presents adequate weight and height according to the physical growth curve of her age group.
In most cases, males with an X-linked form of this condition experience more severe dental abnormalities than affected females.
A year-old, white, female patient, came to the dental office of an extension project called “Gaining Health: Autosomal recessive inheritance means two copies of the gene in each cell are altered.
In the course of the following appointments, the primary teeth with advanced root resorption — which prevented good oral hygiene — were extracted.
The technique was effective for reducing tooth sensitivity. If the patient has primary or mixed dentition, lab-made composite veneers may be provided temporarily, to be replaced by permanent porcelain veneers once the patient has stabilized permanent dentition. Services on Demand Journal.
All of the procedures were preceded by fluoride tooth brushing. N Z Dent J ; Fundamentos interdisciplinares do atendimento de pacientes com necessidades especiais em odontologia. The treatment began with orientations on oral hygiene and eating habits, in addition to supragingival scaling. Bonding agents are used to obliterate dentin tubules by reducing or eliminating tooth sensitivity 11 ,