Results 41 to 50 of about 903 (178)
Acta Medica Alanya, 2017 Osteopoikilosis is a rare bone dysplasia characterized by abnormally enchondral bone maturation, which generally stars to be formed in the childhood and continues in the adulthood. It is generally asemptomatic and it is determined incidentally.
Gökhan Peker +3 more
doaj +1 more source
Buschke-Ollendorff syndrome. A case report with disproportionate short stature
Journal of Clinical and Translational Endocrinology Case Reports, 2021 Objective: To report a Buschke-Ollendorff syndrome case with disproportionate short stature and literature review; recognizing this clinical entity as an infrequent bone dysplasia, which requires a cautious clinical evaluation, bearing in mind not to ...
Ana María Puentes Ortiz +6 more
doaj +1 more source
, 2015 Osteopoikilosis (Spotted Bone, Osteopathia Condensans Disseminata) is a rare autosomal dominant bone disorder with characteristic radiological features. Prevalence has been estimated 1/50.000. The diagnosis usually done according to radiographs which are
Latif Raif, Serap +3 more
core +1 more source
Unusual presentation of osteopoikilosis. [PDF]
, 2013 peer reviewedWe present a case of osteopoikilosis in a 74-year-old woman with hip pain, presenting multiple osteoblastic lesions of the axial skeleton including an osteoblastic large lesion of her left femur.
J Denut +19 more
core +1 more source
Travmatologiâ i Ortopediâ Rossii, 2016 Sclerotic osteodysplasias represent a group of relatively rare diseases; a common feature of them is the diffuse or local bone sclerosis. The reasons for their development are congenital abnormalities of endochondral and intramembranous bone formation ...
A. L. Petrushin +2 more
doaj +1 more source
Multiple myeloma presenting in association with gastric phytobezoar
Clinical Case Reports, Volume 5, Issue 9, Page 1493-1495, September 2017., 2017 We present a rare case of a patient with delayed gastric emptying, gastric phytobezoar formation, and osteosclerotic bone lesions as an atypical association with multiple myeloma. Associated gastric features in myeloma, which include diffuse infiltration, gastric plasmacytomas, or delayed gastric emptying, are rare and have a poor prognosis.
Elizabeth S. Appleton +2 more
wiley +1 more source
A Unique Case of Melorheostosis Presenting with Two Radiologically Distinct Lesions in the Shoulder
Case Reports in Orthopedics, Volume 2017, Issue 1, 2017., 2017 Melorheostosis is a rare, nonhereditary, benign, mesenchymal condition of unknown aetiology affecting the bones and surrounding tissues. A male patient complaining of left shoulder pain, swelling, and mildly limited range of motion has an exclusive combination of the classic dripping wax lesion in the scapula and the myositis ossificans‐like lesion in ...
Ahmed A. Elsheikh +4 more
wiley +1 more source
Osteopoıkılosıs at Hand And Foot Fıngers: Case Report
Acta Medica Alanya, 2018 Osteopoikilosis is a rare and genetical benign bone disease which is not well defined in terms of its phenotypic characteristics. In literature, it is generally stated that it holds large and medium bone metaphyses and phenotypic features are not ...
Rıdvan Altay +2 more
doaj +1 more source
12q14 Microdeletions: Additional Case Series with Confirmation of a Macrocephaly Region
Case Reports in Genetics, Volume 2015, Issue 1, 2015., 2015 To date, there have been only a few reports of patients carrying a microdeletion in chromosome 12q14. These patients usually present with pre‐ and postnatal growth retardation, and developmental delay. Here we report on two additional patients with both genotype and phenotype differences.
Adrian Mc Cormack +7 more
wiley +1 more source
Melorheostosis: Two atypical cases
Indian Journal of Radiology and Imaging, 2014 Melorheostosis is an uncommon mesenchymal dysplasia that rarely affects the axial skeleton.We describe two atypical cases of melorheostosis with classical imaging findings - the first one involving the cervico-dorsal spine with encroachment of left ...
Binit Sureka +5 more
doaj +1 more source