Results 21 to 30 of about 2,787 (193)
Monostotic fibrous dysplasia in a 10-year-old patient
Fibrous dysplasia is a rare congenital bone disorder which manifests as a localized defect in osteoblastic differentiation and maturation with the replacement of normal bone with an abnormal scar-like fibrous connective tissue.
Gayatri Nayanar, Mamatha G S. Reddy
doaj +1 more source
Aggressive Multiple Central Giant Cell Granulomas of the Jaws
Central giant cell granuloma (CGCG) is considered a benign intraosseous lesion with a varied range of clinical features in two subtypes, including aggressive and non‐aggressive lesions. This study presents a 9‐year‐old boy with multiple bilateral CGCG in the mandible without any systemic disease or specific syndrome.
Farnoush Mohammadi +4 more
wiley +1 more source
Epidemiological and Clinical Characteristics of Fibrous Dysplasia of Bone
Objective To describe the epidemiological and clinical characteristics of fibrous dysplasia of bone admitted to a single center in the past 30 years.
XU Hairong +4 more
doaj +1 more source
The explanation of this classification from I to V. Cases presentation for each Type. Objective This study aims to investigate the reliability and clinical outcome of a newly developed classification system for patients with fibrous dysplasia (FD) of the femur and adjacent bones, optimizing its evaluation and management. Methods A total of 205 patients
Yitian Wang +8 more
wiley +1 more source
An unusual case of polyostotic fibrous dysplasia—A case report
Fibrous dysplasia (FD) is a fibro-osseous lesion where normal bone and marrow is replaced with fibrous tissue, resulting in formation of bone that is weak and prone to expansion.
Kiran Suresh Jagtap +3 more
doaj +1 more source
Radiographic classification of coronal plane femoral deformities in polyostotic fibrous dysplasia [PDF]
Fibrous dysplasia of bone is a skeletal dysplasia with a propensity to affect the femur in its polyostotic form, leading to deformity, fracture, and pain.
Boyce, A +5 more
core +1 more source
A case report of McCune–Albright syndrome with hepatic manifestations
Abstract McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jaundice and hyperthyroidism. At the age of 2 years, he suffered from a proximal left femoral fracture.
Mohammad Haddadi +5 more
wiley +1 more source
Whole exome sequencing revealed the underlying genetic mechanisms of osteosarcoma arising from fibrous dysplasia of the jaws. Significant somatic single nucleotide variations, including TP53, ROS1 AND CHD8, as well as large amounts of somatic copy number alterations were demonstrated.
Ruirui Shi +6 more
wiley +1 more source
Secondary amenorrhea in a case of gonadotropin independent precocious puberty: McCune-Albright syndrome [PDF]
Precocious puberty may be gonadotropin dependent or gonadotropin independent and due to a myriad of causes including syndromic association. McCune-Albright syndrome (MAS) is a rare disorder, characterized by the triad of precocious puberty, polyostotic ...
Jayaraman, Sangumani +4 more
core +2 more sources
Fibrocartilaginous dysplasia: What do we know so far?
Fibrocartilaginous dysplasia has been described as a rare variant of fibrous dysplasia. This lesion will appear in imaging as ground glass matrix similar to fibrous dysplasia, but it will also show rings and arcs calcifications. In turn, this can lead to
Asma Alshalan, MD +3 more
doaj +1 more source

