Results 151 to 160 of about 1,058,904 (200)

The use of denosumab in rare bone diseases in adults: a systematic review from the ECTS Rare Bone Disease Action Group.

J Clin Endocrinol Metab
Bulaicon OO, van Haalen FM, Clunie GPR, Grasemann C, Lems WF, Makras P, Mortier G, Oheim R, Raimann A, Siggelkow H, Tabacco G, van der Wal RJP, de Witte PB, Appelman-Dijkstra NM.   +13 more
europepmc   +1 more source

Surgical Management of a Case of Frontoparietal Fibrous Dysplasia. [PDF]

Cureus
Moussa A, Adraoui A, Haouane MA, Ounjar A, Akhaddar A, Belfquih H.   +5 more
europepmc   +1 more source

Clonal megakaryocyte dysplasia with normal blood values: a covert, thrombosis-prone, early myeloproliferative neoplasm. [PDF]

Haematologica
Barosi G, Rosti V, Campanelli R, Massa M, Abbà C, Carolei A, Catarsi P, Inzoli A, Pergola L, Barbui T, Tatarelli C, Finazzi MC, Condorelli A, Salmoiraghi S, Rambaldi A, Gianatti A, De Stefano V, Gallì A, Gandossini M, Bardelli M, Gale RP, Malcovati L.   +21 more
europepmc   +1 more source

Osteomesopyknosis: A Bone-Sclerosing Disorder that May be Confused with Bone Metastases. [PDF]

Calcif Tissue Int
Riancho JA, Del Real A, Vega AI, Landeras R, Ferrerira A, Ferreira AC, Sainz J, Quirce R, de Castro EM.   +8 more
europepmc   +1 more source

Radiographic and Histopathological Characteristics of Chronic Nonbacterial Osteomyelitis of the Mandible in Pediatric Patients: Case Series. [PDF]

Diagnostics (Basel)
Barayan M, Abdel Wahed N, Helal N, Komo HA, Iskanderani D, Alansari R, Alhindi NA, Alhelo AF, Khalifa H, Sabban H.   +9 more
europepmc   +1 more source

Sclerosing Bone Dysplasias [PDF]

Best Practice & Research Clinical Endocrinology & Metabolism, 2018
The group of sclerosing bone dysplasia's is a clinically and genetically heterogeneous group of rare bone disorders which, according to the latest Nosology and classification of genetic skeletal disorders (2015), can be subdivided in three subgroups; the neonatal osteosclerotic dysplasias, the osteopetroses and related disorders and the other ...
Wim Van Hul, Eveline Boudin
exaly   +4 more sources

A Novel Sclerosing Skeletal Dysplasia With Mixed Sclerosing Bone Dysplasia, Characteristic Syndromic Features, and Clinical and Radiographic Evidence of Male–Male Transmission

American Journal of Medical Genetics, Part A, 2012
AbstractWe report on a father and his 4‐year‐old son sharing a characteristic dysmorphic facial phenotype (including hyperteleroism, prominent forehead, and wide nasal bridge), macrocephaly, hearing loss, palatal clefting, developmental delay, hypotonia and bony abnormalities including marked cranial sclerosis and sclerosis of the ribs and long bones ...
Dusica Babovic-Vuksanovic, Kristen B Thomas, Larry A Binkovitz   +2 more
exaly   +4 more sources

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Sclerosing Bone Dysplasias: Genetic and Radioclinical Features

European Radiology, 2000
Although knowledge of basic genetics in the field of sclerosing bone dysplasias is progressing, the radiologist still plays a pivotal role in the diagnosis of this relatively poorly understood group of disorders. Based on a target site approach, these anomalies are classified into three groups.
Wim Van Hul, F M Vanhoenacker, S C Hill
exaly   +4 more sources

Melorheostosis: A Rare Sclerosing Bone Dysplasia

Current Osteoporosis Reports, 2017
Melorheostosis is a rare sclerosing bone dysplasia that affects both cortical bone and adjacent soft tissue structures in a sclerotomal distribution. In this review, we describe the natural history, radiological features, proposed pathogenesis, and management options for this debilitating condition.Since its first description in 1922, about 400 cases ...
Bart L Clarke, Anupam Kotwal
exaly   +3 more sources

Ophthalmological Complications in the Sclerosing Bone Dysplasias

Ophthalmic Paediatrics and Genetics, 1985
The sclerosing bone dysplasias are a group of rare genetic disorders in which overgrowth of the cranio-facial skeleton causes a variety of ophthalmological complications. During the past decade more than 100 South Africans with conditions in this category have been investigated and their ocular manifestations have been appraised.
Peter Beighton, H Hamersma
exaly   +3 more sources