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Idiopathic osteosclerosis, also known as enostosis or dense bone island, is a condition which may be found around the roots of a tooth, usually a premolar or molar. [2] It is usually painless and found during routine radiographs as an amorphous radiopaque (light) area around a tooth.
Floating–Harbor syndrome, also known as Pelletier–Leisti syndrome, is a rare disease with fewer than 50 cases described in the literature. [1] It is usually diagnosed in early childhood and is characterized by the triad of proportionate short stature with delayed bone age, characteristic facial appearance, and delayed speech development.
Osteosclerosis is a disorder characterized by abnormal hardening of bone and an elevation in bone density. It may predominantly affect the medullary portion and/or cortex of bone. Plain radiographs are a valuable tool for detecting and classifying osteosclerotic disorders. [1] [2] It can manifest in localized or generalized osteosclerosis.
Condensing osteitis, also known as focal sclerosing osteomyelitis, is a rare periapical inflammatory condition characterized by the formation of sclerotic bone near the roots of premolars and molars. This condition arises as a response to dental infections, such as periapical pulp inflammation or low-intensity trauma.
Periapical radiographs can locate radiopaque structures in proximity to the root which can appear as dense bone islands or periapical osseous dysplasia in cases of hypercementosis. [9] The majority of affected teeth appear club-shaped due to cemental hyperplasia diffusing in a variety of severities. Most appear in the apical third of the root. [10]
Fibrodysplasia ossificans progressiva (/ ˌ f aɪ b r oʊ d ɪ ˈ s p l eɪ ʒ (i) ə ɒ ˈ s ɪ f ɪ k æ n z p r ə ˈ ɡ r ɛ s ɪ v ə /; [1] abbr. FOP), also called Münchmeyer disease or formerly myositis ossificans progressiva, is an extremely rare connective tissue disease in which fibrous connective tissue such as muscle, tendons, and ligaments turn into bone tissue (ossification).
It is due to a defect in the RUNX2 gene which is involved in bone formation. [1] Diagnosis is suspected based on symptoms and X-rays with confirmation by genetic testing . [ 4 ] Other conditions that can produce similar symptoms include mandibuloacral dysplasia , pyknodysostosis , osteogenesis imperfecta , and Hajdu-Cheney syndrome .
A biopsy can be useful in ruling out other possible diagnoses, like a bone tumor. [2] A variety of benign and malignant bone abnormalities, including as cysts, osteoid osteoma, giant cell tumors, chondroblastomas, and Ewing sarcoma, are included in the differential diagnosis of Brodie abscess. [3]