Nihan Aksakallı

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PURPOSE The purpose of the present study was to evaluate the clinical and histopathologic aspects of different types of odontomas. MATERIALS AND METHODS One hundred sixty odontoma cases sent to the Institute of Oncology, Department of Tumor Pathology, Istanbul University from 1971 through 2010 were investigated. These tumors were compared by age of(More)
  • PRIKAZ SLU»AJA, CaSe rePort, +4 authors ACtA STOMATOLOGICA
  • 2010
Adresa za dopisivanje Dr.Amila Brkić Sveučilište u Sarajevu Stomatološki fakultet Bolnička 4a, 1000 Sarajevo Bosna i Hercegovina Sažetak Prekobrojni zubi nisu česta pojava, osobito ako nisu povezani s kleidokranijalnom displazijom, rascjepom usne i nepca ili sindromima poput Gardnerova. Naizgled zdrava 22-godišnja pacijentica bila je(More)
Pilomatricoma is a relatively rare tumour of the skin derived from primitive basal cells of epidermis that differentiate into hair matrix cells. It comprises approximately 1% of all benign skin tumours. The most common sites for pilomatricomas are the head, neck and upper extremities. A 44-year-old woman, admitted to our department, underwent an(More)
OBJECTIVES Pediatric odontogenic lesions are rare clinical entities and are not well addressed in the otolaryngology literature. Knowledge of the biologic and clinical behavior of these lesions and their basic features such as location and age are key aspects for otolaryngologists in developing an early clinical differential diagnosis, such that they can(More)
Ehlers-Danlos syndrome is an autosomal dominant hereditary disorder of connective tissue, while familial gigantiform cementoma is a condition that usually manifests as multiple radiopaque cementum-like masses throughout the jaws. This case report discusses the oral management and prosthetic rehabilitation of two patients presenting familial gigantiform(More)
Frank-ter Haar syndrome is a genetic disease that is transmitted by autosomal recessive pattern with characteristic features such as megalocornea or glaucoma, a prominent coccyx, heart defects, developmental delays, brachycephaly, a wide anterior fontanel, finger flexion deformities, full cheeks and micrognathia. Dentomaxillofacial features of this syndrome(More)
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