Results 81 to 90 of about 903 (178)

REASONED APPROACH TO MULTIPLE OSTEOSCLEROTIC LESIONS. COMBINED DIAGNOSTIC IMAGING IN A CASE OF OSTEOPOIKILOSIS

open access: yes, 2005
The case of a female patient who had undergone mastectomy for infiltrating ductal carcinoma and come to the Orthopedics Division for lumbosacral pain unresponsive to conventional treatment is discussed.
MARANO P.   +4 more
core  

Osteopoikilosis: Report of a familial case

open access: yes, 1994
We describe four members of a family in which the clinical and radiological findings lead to consider the diagnosis of osteopoikilosis. The symptoms in all affected members were only those referred to as typical radiological features; these features ...
Sanchez-Corona, J.   +3 more
core   +1 more source

Osteopoikilia: presentation of two cases

open access: yesActa Médica del Centro, 2010
The osteopoikilosis is a rare illness characterized by an alteration of the bone remodeling. The case of two patients, members of the same family (mother and son), who suffered from this illness, is presented here.
Damaris Pérez Betancourt   +2 more
doaj  

MIXED SCLEROSING BONE DYSTROPHIES

open access: yes, 1964
1. A Nigerian patient with radiographic features of osteopathia striata, osteopoikilosis and melorheostosis is reported. Also radiographs of a patient from the Radiographic Museum of the Institute of Orthopaedics at the Royal National Orthopaedic ...
Geoffrey F. Walker
core   +1 more source

Buschke-Ollendorff Syndrome(증례 보고)

open access: yes, 1996
The osteopoikilosis is commonly known as harmatoma in which metaphyseal and epiphyseal area of long bones and the bone of pelvis, hands, feet and et al, contain islands of dense cortical bone with normal Harversian system without any symptoms.
이, 은소   +6 more
core   +1 more source

Osteopoikilosis (A Case Report)

open access: yesEurasian Journal of Medicine, 2019
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Şefik Güney
doaj  

P60 | Osteopoikylosis and secondary hyperparathyroidism: an unusual association of rare diseases

open access: yesItalian Journal of Medicine
Background: Osteopoikilosis (OPK) is a rare bone disease with a prevalence of 1/50,000. It’s usually diagnosed incidentally by radiographic examinations. The etiopathogenesis is still unclear. In Literature OPK is described as frequently associated with
doaj   +1 more source

Familial osteopoikylosis A report on a rare case

open access: yesActa Orthopaedica et Traumatologica Turcica
A case of typical osteopoikilosis has been presented with radiographs of the whole skeletal system. Family history revealed the presence of typical skeletal disorders in both the patient s father and brother.
Dilek Onel, S. Fikret Tuzun
doaj  

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