منابع مشابه
Familial Polythelia associated with dental anomalies: a case report
Polythelia has been defined as the presence of supernumerary nipples without accessory glandular tissue. Usually, these growths follow imaginary mammary lines running from the armpits to the groin. Although the presence of dental anomalies may occasion only a simple cosmetic problem with specific clinical considerations, the association with familial polythelia has been scarcely reported. This ...
متن کاملNovel dental anomalies associated with congenital contractural arachnodactyly: a case report.
Congenital contractural arachnodactyly (CCA) is an inherited disorder of connective tissue similar to Marfan's syndrome. The craniofacial and oral features of a young girl with CCA are described. The patient has the typical features of CCA as well as some additional dental anomalies which have not previously been reported with this syndrome. These include banded pitted enamel hypoplasia and hyp...
متن کاملMultiple Dental Anomalies in Primary and Permanent Dentition: A Case Report
Dental anomalies are rare findings that may affect development of occlusion and early intervention may be required. Here, a case of multiple anomalies in primary and permanent dentitions is reported. The patient referred to the dental center with the chief complaint of multiple tooth decay. In the oral examination, the rare case of triplication between the right geminated man-dibular A and...
متن کاملAplasia cutis congenita associated with multiple congenital anomalies: case report.
INTRODUCTION Aplasia cutis congenita (ACC), is a rare anomaly presenting with a solitary scalp lesion of skin abrasion. Lesions can be multiple and on different surfaces of the body but are mostly seen on the scalp (%70) as a solitary lesion. As it is a rare disease, we aimed to describe our case with ACC. CASE REPORT Our case was a newborn infant with a large full thickness skin and skull de...
متن کاملDiphallia with Associated Anomalies: A Case Report and Literature Review
Diphallia or penile duplication is an extremely rare congenital anomaly. It occurs once in every 5.5 million live births. The extent of penile duplication and the number of associated anomalies vary greatly, ranging from a double glans from a penis with no associated anomaly up to complete penile duplication associated with multiple anomalies. Here, we report a 12-year-old boy with complete bif...
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ژورنال
عنوان ژورنال: Journal of Applied Oral Science
سال: 2005
ISSN: 1678-7757
DOI: 10.1590/s1678-77572005000400021