Results 11 to 20 of about 1,058,904 (200)
Radiology Case Reports, 2018 Melorheostos is a rare sclerosing bone dysplasia, characterized by cortical and medullary hyperostosis with typical “dripping candle wax” appearance, usually involving the long bones.
Alexandre Semionov +2 more
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MELORHEOSTOSIS AT LEFT LOWER LIMB OF A 22 YEARS OLD FEMALE: A RARE CASE
National Journal of Medical Research, 2020 Sclerosing bone dysplasias are skeletal abnormalities of varying severity with a wide range of radiologic, clinical, and genetic features. It is divided into Hereditary and Non-hereditary.
Thomson Manurung +3 more
doaj +1 more source
A new familial sclerosing bone dysplasia [PDF]
Journal of Bone and Mineral Research, 2010 Abstract Osteoscleroses are a heterogeneous group of bone remodeling disorders characterized by an increase in bone density. Here we report on a consanguineous Lebanese family in which two sisters, aged 39 and 36 years, exhibit a severe genu varum, a square-face appearance, high forehead, slight proptosis of the eyes, symmetric ...
Chouery, E. +11 more
openaire +6 more sources
Mixed Sclerosing Dysplasia of the Bone Associated with Ovarian and Skin Problems
Clinical Orthopaedics and Related Research, 2005 The clinical, radiologic, histopathologic, and genetic features of a sclerosing bone dysplasia found in three members of a family are described. The bone disorder affected all metaphyseal-diaphyseal regions of all long bones, the skull, and three metacarpals. All affected members also had ichthyosis vulgaris and premature ovarian failure.
Degirmenci, B. +4 more
openaire +4 more sources
Combined Fronto-orbital Contouring and Orthognathic Surgery in Craniometaphyseal Dysplasia
Plastic and Reconstructive Surgery, Global OpenSummary:. Craniometaphyseal dysplasia is a rare congenital sclerosing skeletal dysplasia that presents with facial dimorphism and is clinically described by prominent supraorbital bridges, severe retrognathia, and respiratory problems.
Bruno Nifossi Prado, DDS, MSc +1 more
doaj +2 more sources
Türk Osteoporoz Dergisi, 2010 Osteopoikilosis (OPK) is an asymptomatic, rare bone dysplasia. It causes an increase in bone density. The etiology and pathogenesis is unknown. OPK is generally diagnosed incidentally on plain radiographies which were performed for other locomotor system
Asylbek Kaparov +3 more
doaj +1 more source
Use of Fibrin Sealant Combined With Demineralized Freeze-Dried Bone Allograft in the Management of a Recurrent Mandibular Aneurysmal Bone Cyst: A Case Report. [PDF]
Clin Case RepABSTRACT Recurrent aneurysmal bone cysts of the jaw present significant therapeutic challenges. This case suggests that fibrin sealant combined with demineralized freeze‐dried bone allograft, as an adjunct to curettage, may offer a conservative option in selected young patients after failure of conventional therapies. Further studies are needed.
Mokhtari Z, Politis C, Shall F.
europepmc +2 more sources
Familiar osteopoikilosis: Case report with differential diagnosis and review of the literature
Clinical Case Reports, 2021 Osteopoikilosis (OP) is a rare autosomal dominant sclerosing bone disease, caused by heterozygous mutations in the LEMD3 gene. It is characterised by numerous focal lamellar bone compact deposits in the spongiosa.
Agostino Gaudio +10 more
doaj +1 more source
JBMR Plus, 2023 Osteosclerotic metaphyseal dysplasia (OSMD) is a very rare autosomal‐recessive disease caused by mutations in the leucine‐rich repeat kinase 1 (LRRK1) gene.
Evert F.S. vanVelsen +3 more
doaj +1 more source
Sphenoid Bone Dysplasia: A Rare Cause of Compressive Optic Neuropathy Mimicking Glaucoma [PDF]
, 2023 Fibrous dysplasia is a benign, rare bone disease in which bone is replaced by fibro-osseous tissue to varying degrees. It can present differently depending on the amount of compression caused by the fibro-osseous tissue. Patients are usually asymptomatic,
Pelin Kıyat +7 more
core +1 more source