Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report
Osteopetrosis is a rare inherited genetic disease characterized by sclerosis of the skeleton caused by the absence or malfunction of osteoclasts. Three distinct forms of the disease have been recognized, autosomal dominant osteopetrosis being the most common. Autosomal dominant osteopetrosis exhibit...
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doaj-f7bef4d3139a461a9ffec3de3f59de422021-07-02T05:34:20ZengHindawi LimitedCase Reports in Dentistry2090-64472090-64552013-01-01201310.1155/2013/707343707343Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case ReportPriyanka Kant0Neelkamal Sharda1Rahul R. Bhowate2Department of Oral Medicine and Radiology, Manav Rachna Dental College, Sector 43, Aravalli Hills, Delhi-Surajkund Road, Faridabad, Haryana 121001, IndiaDepartment of Oral Medicine and Radiology, Manav Rachna Dental College, Sector 43, Aravalli Hills, Delhi-Surajkund Road, Faridabad, Haryana 121001, IndiaDepartment of Oral Medicine and Radiology, Sharad Pawar Dental College and Hospital, Sawangi, Wardha, Maharashtra 442001, IndiaOsteopetrosis is a rare inherited genetic disease characterized by sclerosis of the skeleton caused by the absence or malfunction of osteoclasts. Three distinct forms of the disease have been recognized, autosomal dominant osteopetrosis being the most common. Autosomal dominant osteopetrosis exhibits a heterogeneous trait with milder symptoms, often at later childhood or adulthood. The aim of this case report is to present the clinical and radiographic features of a 35-year-old female patient with autosomal dominant osteopetrosis type II who exhibited features of chronic generalised periodontitis, and the radiographs revealed generalised osteosclerosis and hallmark radiographic features of ADO type II, that is, “bone-within-bone appearance” and “Erlenmeyer-flask deformity.”http://dx.doi.org/10.1155/2013/707343 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Priyanka Kant Neelkamal Sharda Rahul R. Bhowate |
spellingShingle |
Priyanka Kant Neelkamal Sharda Rahul R. Bhowate Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report Case Reports in Dentistry |
author_facet |
Priyanka Kant Neelkamal Sharda Rahul R. Bhowate |
author_sort |
Priyanka Kant |
title |
Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report |
title_short |
Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report |
title_full |
Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report |
title_fullStr |
Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report |
title_full_unstemmed |
Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report |
title_sort |
clinical and radiological findings of autosomal dominant osteopetrosis type ii: a case report |
publisher |
Hindawi Limited |
series |
Case Reports in Dentistry |
issn |
2090-6447 2090-6455 |
publishDate |
2013-01-01 |
description |
Osteopetrosis is a rare inherited genetic disease characterized by sclerosis of the skeleton caused by the absence or malfunction of osteoclasts. Three distinct forms of the disease have been recognized, autosomal dominant osteopetrosis being the most common. Autosomal dominant osteopetrosis exhibits a heterogeneous trait with milder symptoms, often at later childhood or adulthood. The aim of this case report is to present the clinical and radiographic features of a 35-year-old female patient with autosomal dominant osteopetrosis type II who exhibited features of chronic generalised periodontitis, and the radiographs revealed generalised osteosclerosis and hallmark radiographic features of ADO type II, that is, “bone-within-bone appearance” and “Erlenmeyer-flask deformity.” |
url |
http://dx.doi.org/10.1155/2013/707343 |
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