Bone Fibrosis Dysplasia - Gastrointestinal Case Report
نویسندگان
چکیده مقاله:
Un cas de fihreuse dysplasie evoluant dcpuis dix ans a ete observe a l'hopital farahnaz de l'universite Melli de Teheran. La particu-larite in terssante de cettc patiente est tout d'abord la clegenerscence kystiquc de foyer de l'os iliaque droit et la multitude des fractures des membres ayant consolide dans des positions v1cieusc spon tanement. Presence d'un foyer temporal gauchf! de .forme sclerotique avec des signes de compression ophtalmique gauche.
منابع مشابه
Dentin Dysplasia: ARare Case Report
Introduction: Dentin Dysplasia is one of the rare hereditary diseases that the enamel is normal, but it also affects the dentin and the shape of the tooth pulp. Due to the low prevalence of this disease, a case of dentin dysplasia with the classical and atypical dentin dysplasia type 1 is presented. Case presentation:A 11-year-old girl with the mobility of lower central teeth that has severe ...
متن کاملOral Submucous Fibrosis: a case report
We describe an interesting case of oral sub mucous fibrosis accompanied by severe trismus in a 23 years old man. The patient had initially been diagnosed as having internal derangement of the temporomandibular joint and conservative treatment had failed to decrease the symptoms. Despite extremely limited temporomandibular joint movement, cone beam computed tomography revealed no important abnor...
متن کاملDiastrophic dysplasia: case report.
This report describes the clinical features of an 11-yearold male whose genetic evaluation supports the diagnosis of diastrophic dysplasia. A professional team evaluated and treated him with regard to facial development, various physical problems, and pediatric dental management of his intraoral conditions. Cardiopulmonary function often is compromised because of kyphoscoliosis. This along with...
متن کاملSegmental odontomaxillary dysplasia (hemimaxillofacial dysplasia): case report.
Segmental odontomaxillary dysplasia (SOD) has been delineated from other bone and odontogenic dysplasias, and only recently has been described as a separate entity.' This condition was first introduced as hemimaxillofacial dysplasia (HD) by Miles et al. in 1987.' Reports have appeared directed primarily at oral and maxillofacial surgeons and oral pathologists, so the condition may be relatively...
متن کاملBone Metastases from Gastrointestinal Stromal Tumor: A Case Report
Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal neoplasms of the gastrointestinal tract. Their most common metastatic sites are the liver and the peritoneum, but GISTs rarely metastasize to the bones. We report a case of a 58-year-old man with sternoclavicular joint metastasis from a GIST manifesting 28 months after surgical resection of the small intestine tumor. We wil...
متن کاملCleidocranial Dysplasia: A Case Report
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease. CCD is caused by mutation in the gene on 6p21 encoding transcription factor CBFA1, i.e. runt-related transcription factor 2(RUNX2). The disease is characterized by a persistently open anterior fontanelle and skull sutures, hypoplastic or aplastic clavicles, dental abnormalities, short stature, a wide pubic symphysis, a...
متن کاملمنابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ذخیره در منابع من قبلا به منابع من ذحیره شده{@ msg_add @}
عنوان ژورنال
دوره 3 شماره 4
صفحات 332- 337
تاریخ انتشار 1975-07
با دنبال کردن یک ژورنال هنگامی که شماره جدید این ژورنال منتشر می شود به شما از طریق ایمیل اطلاع داده می شود.
میزبانی شده توسط پلتفرم ابری doprax.com
copyright © 2015-2023