Asymmetrical tooth defects observed in hypoplastic primary teeth and amelogenesis imperfecta: case reports.

نویسندگان

  • A L Symons
  • J P Gage
چکیده

Two rare cases of asymmetrical tooth destruction affecting the primary dentition and 1 case of hypoplastic, vertical striping X-linked amelogenesis imperfecta which affects the permanent dentition in an asymmetrical manner, are presented. The etiology of the conditions are discussed with respect to inheritance, preeruptive and posteruptive influences. The asymmetrical gross tooth destruction reported in the 2 primary dentitions may be multifactorial in origin but genetic influences cannot be excluded. Factors that may disturb ameloblasts and result in their producing hypoplastic enamel include genetic causes, nutritional deficiency, maternal illnesses, birth injury, and trauma (Kreshover et al. 1958). This paper presents 2 unusual cases of tooth destruction and 1 case of hypoplastic amelogenesis imperfecta and discusses the possible reasons for the atypical distribution of defects. Variations in the number and form of teeth are, in general, genetically determined, but modifications may also arise as a result of a number of other influences. For example, the absence of teeth such as lateral incisors or third molars may be an inherited anomaly--as may other conditions such as amelogenesis imperfecta and dentinal dysplasia. On the other hand, pre-eruptive influences such as systemic illnesses or local trauma may result in alteration of the tooth bud components during tooth formation. Dental structures generally are well protected from damaging influences during intrauterine life but children with premature or traumatic births tend to have a higher incidence of dental anomalies in the primary dentition (Rosenzweig and Sahar 1962). Kreshover et al. (1958) examined the prevalence of developmental dental abnormalities in primary teeth and concluded they were more common than previously thought. Microscopic examination of the teeth of both jaws showed a prominent incremental line extending over the incisal and occlusal portions of the deciduous anterior and posterior teeth. Rosenzweig and Sahar (1962) and Kreshover et al. (1958) found that children with hypoplastic teeth had a greater dmf rate than those without hypoplasia and suggested that hypoplastic teeth may be more susceptible to dental caries than normally calcified teeth. Case 1 A 4-year-old Caucasian female was referred to the pedodontic clinic for management of gross enamel erosion and severe wear of the primary teeth on

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Hypoplastic Amelogenesis Imperfecta type GI (enamel agenesis): a case report

Background and Aim: Amelogenesis Imperfecta is a hereditary complication that affects the quality and quantity of tooth enamel. This disease usually affects both deciduous and permanent dentition and causes various abnormalities such as unaesthetic appearance, dental sensitivity, and severe attrition. The incidence of this condition is estimated at 1 in 14,000 people. At the moment, there are n...

متن کامل

Enamel 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 کامل

CASE REVIEW Clinical diagnosis and management s rategies of amelogenesis imperfecta variants

Amelogenesis imperfecta (AI) is a group of inherited disorders primarily affecting dental enamel. Variants of AI generally are classified as hypoplastic, hypocalcified, or hypomaturation types based on the primary enamel defect. The aim of this study was to analyze the clinical presentations, diagnostic features, and clinical complications of different variants of AI. Thirty-two patients from 1...

متن کامل

Pre-Eruptive Coronal Resorption and Congenitally Missing Teeth in a Patient with Amelogenesis Imperfecta: A Case Report

This clinical report describes a male with autosomal recessive generalized hypoplastic amelogenesis imperfecta. This case is unusual in coronal resorptions prior to tooth eruption. This finding has been reported in some cases of autosomal recessive, autosomal dominant and X linked amelogenesis imperfecta (AI). In reported cases, the defects were usually small and occurred in a maximum of 2 teet...

متن کامل

An Interdisciplinary Approach for Rehabilitating a Patient with Amelogenesis Imperfecta: A Case Report

Amelogenesis imperfecta (AI) has been defined as a group of hereditary enamel defects. It can be characterized by enamel hypoplasia, hypomaturation, or hypocalcification of the teeth. AI may be associated with some other dental and skeletal developmental defects. Restoration for patients with this condition should be oriented toward the functional and esthetic rehabilitation. This clinical repo...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Pediatric dentistry

دوره 9 2  شماره 

صفحات  -

تاریخ انتشار 1987