AMELOGENESE IMPERFEITA PDF

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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After the physical examination, a treatment plan that covered both functional and aesthetic aspects was drawn up.

Stomatos – Amelogenese imperfecta em uma criança com paralisia cerebral

However, the issues linked to the dental caregivers are usually not technical, but rather related to human factors, such as moral, philosophical and psychological aspects The restraint of the subject is precisely indicated for cases in which neuromotor disorders lead the patient to make involuntary movements. In addition to the cerebral palsy systemic frame, this patient presented amelogenesis imperfecta, a malformation of the dental enamel that affects both primary and permanent dentition Check this box if you wish to receive a copy of your message.

All of the procedures were preceded by fluoride tooth brushing. The case shows that it is possible to perform complex dental care of disabled patients in an outpatient environment.

Orphanet: Platispondilia amelogenese imperfeita

The patient has a finger-sucking habit of her left thumb, both in stressful and in pleasant situations, causing anterior open bite. Noninvasive and multidisciplinary approach to the functional and esthetic rehabilitation of amelogenesis imperfecta: Clin Oral Invest ; The diagnosis of Hypoplastic Amelogenesis Imperfecta was confirmed based on the anamnesis and physical and radiographic examinations, since the enamel presented reduced thickness, with imperefita and pits.

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The choice of this protocol was based on sensitivity control and reduced clinical time, because the patient had attention-deficit hyperactivity disorder and had no loss of vertical dimension. Microtensile bond strength to enamel affected by hypoplastic amelogenesis imperfecta.

There is a large array of possibilities for treating AI, with a variety of restorative materials and methods; it is up to the dental caregiver to select the most appropriate ones The crown had to be adapted by cutting its cervical border with the aid of curved scissors and scalpel Figure 6.

Interventions for the restorative care of amelogenesis imperfecta in children and adolescents.

A manifestation of amelogenesis imperfecta known as “snow capping” is confined to the outer prismless enamel layer. It is predominantly a sensorimotor dysfunction, involving disorders in muscle tonus, posture, and voluntary movement 4.

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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. Health care resources for this disease Expert centres 50 Diagnostic tests 5 Patient organisations 15 Orphan drug s 0.

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For these restorations, prefabricated acetate crowns were selected. The dental caregiver must be aware of speech disorders and also lack of correspondence between the chronological age of the patient and his actions. This page was last edited on 27 Octoberat These teeth are more prone to abrasion, which causes loss of vertical dimension, with aesthetic impairment and dentin exposure, possibly leading to sensitivity to temperature changes.

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These episodes may be related to the development of the cerebral palsy. Teeth 12, 22, 31, 32, 41 and 42 were also restored following the same abovementioned steps. J Orthod Sci ;3: Amelogenesis imperfecta-nephrocalcinosis syndrome Prevalence: A study of the dental treatment needs of children with disabilities in Melbourne Australia.

Dilaceration Regional odontodysplasia Turner’s hypoplasia Enamel hypoplasia Ectopic enamel. Mutations in the ENAM gene are the most frequent known cause and are most commonly inherited in an autosomal dominant pattern.

Amelogenesis imperfecta

At the buccal, lingual or palatal and occlusal faces Figs. Revista ABO Nacional ; In most cases, males with an X-linked form of this condition experience more severe dental abnormalities than affected females.

N Z Dent J ; Esthetic dental anomalies as motive for bullying in schoolchildren.