نتایج جستجو برای: multicentric carpotarsal osteolysis

تعداد نتایج: 6867  

Background: We sought to characterize humeral-sided radiographic changes at a minimum of 2 years after reverseshoulder arthroplasty (RSA) to determine their association with specific implantation techniques.Methods: The immediate and most recent postoperative anteroposterior radiographs of 120 shoulders with primary RSAand a minimum of 2-years of radiographic follow-up were an...

Journal: :Journal of clinical and diagnostic research : JCDR 2013
Ankur Singh Seema Kapoor Gaurav Pradhan

Spondylocarpotarsal synostosis syndrome (SSS) is an autosomal recessive condition which is characterized by short stature, a carpotarsal coalition and a vertebral fusion, but without any rib anomaly. We are presenting a 7- year- old boy, who had uroliathiasis with the spondylocarpotarsal synostosis syndrome. This association, to the best of our knowledge, has not been reported so far.

2016
Karin Pichler Daniela Karall Dieter Kotzot Elisabeth Steichen-Gersdorf Alexandra Rümmele-Waibel Laureane Mittaz-Crettol Julia Wanschitz Luisa Bonafé Kathrin Maurer Andrea Superti-Furga Sabine Scholl-Bürgi

Multicentric osteolysis, nodulosis and arthropathy (MONA) spectrum disorder is a rare inherited progressive skeletal disorder caused by mutations in the matrix metalloproteinase 2 (MMP2) gene. Treatment options are limited. Herein we present successful bisphosphonate therapy in three affected patients. Patients were treated with bisphosphonates (either pamidronate or zoledronate) for different ...

2016
CK Chan Razif-MA Mohamed AA Azlina MM Azhar

Multicentric disappearing bone disease, or Gorham disease, is a rare entity. A middle age woman, presented to us with left sided antalgic gait and severe bony deformity of her left knee. Radiograph revealed massive bone defect of the medial condyle of the left tibia with subluxation of the knee joint. She was scheduled for knee replacement in six months. However, she developed another lesion ov...

Journal: :Annals of the Rheumatic Diseases 2023

Background Multicentric osteolysis, nodulosis and arthropathy (MONA) spectrum disorder is a rare inherited progressive skeletal caused by mutations in the matrix metalloproteinase 2 (MMP2) gene. It characterized multiple peripheral wide metacarpals, osteoporosis, joint contractures, short stature, subcutaneous nodules as well coarse face, skin lesions/hirsutism ocular cardiac manifestations. Th...

Journal: :Journal of medical genetics 2000
T J De Ravel G Matthijs M Holvoet C Wouters E Legius J P Fryns

Journal: :middle east journal of cancer 0
heba g. el-sheredy department of cancer management and research, medical research institute, alexandria university, alexandria, egypt sanaa a. el-benhawy department of radiation sciences, medical research institute, alexandria university, alexandria, egypt khaled matrawy department of radiodiagnosis, medical research institute, alexandria university, alexandria, egypt rabie ramadan department of surgery, medical research institute, alexandria university, alexandria, egypt yasser hamed department of surgery, medical research institute, alexandria university, alexandria, egypt

background: although multifocal and multicentric breast cancers are a common entity, their clinical behavior is not well characterized. with the widespread use of mammographic screening and improved sensitivity of imaging modalities, the detection of multifocal and multicentric breast cancers is likely to continuously increase. many studies have consistently shown a correlation between multifoc...

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