Results 211 to 220 of about 4,018 (255)
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Radiology, 1952
Hereditary multiple exostoses is a familial disturbance in the growth of cartilaginous bone tissue, most marked at the diaphyso-epiphyseal junction of the long bones. Until the report of Ehrenfried (1) in 1917, mention of this disease was relatively infrequent in the American literature, but since that time numerous cases have been reported (2).
William H. Robinson +2 more
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Hereditary multiple exostoses is a familial disturbance in the growth of cartilaginous bone tissue, most marked at the diaphyso-epiphyseal junction of the long bones. Until the report of Ehrenfried (1) in 1917, mention of this disease was relatively infrequent in the American literature, but since that time numerous cases have been reported (2).
William H. Robinson +2 more
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New England Journal of Medicine, 1949
HEREDITARY multiple exostoses are a distinct clinical entity more frequently encountered than is generally appreciated. We have recently had the opportunity of studying 4 members of a Negro family who had the condition. Few cases occurring in Negroes are reported in the American literature.1 2 3 To our knowledge this is the first Negro family studied ...
Paul D. Doolan, Joseph Rose
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HEREDITARY multiple exostoses are a distinct clinical entity more frequently encountered than is generally appreciated. We have recently had the opportunity of studying 4 members of a Negro family who had the condition. Few cases occurring in Negroes are reported in the American literature.1 2 3 To our knowledge this is the first Negro family studied ...
Paul D. Doolan, Joseph Rose
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Hereditary Multiple Exostoses with Pseudoaneurysm
CardioVascular and Interventional Radiology, 2007A 16-year-old male patient with hereditary multiple exostoses (HME) was found to have a pseudoaneurysm of the left popliteal artery caused by osteochondroma in the lower femur. The diagnosis was confirmed by ultrasound, magnetic resonance imaging and magnetic resonance angiography without the need to perform an angiogram. The osteochondroma was excised
Moaath Alsmady +5 more
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Multiple hereditary exostoses and enchondromatosis
Best Practice & Research Clinical Rheumatology, 2020Multiple hereditary exostoses (MHE) and enchondromatosis are rare multifocal benign disorders usually causing skeletal deformities appearing already in childhood. MHE is a dominant autosomal inherited disorder characterized by multiple osteochondromas (exostoses) growing outward from the metaphyses of long bones as well as from flat bones.
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Hereditary multiple exostoses and enchondromatosis
Best Practice & Research Clinical Rheumatology, 2008Hereditary multiple exostoses (HME) is an autosomal-dominant disorder characterized by the development of benign tumours, multiple osteochondromas (exostoses), growing outward from the metaphyses of long bones. Birth prevalence is estimated to be one in 50,000, and the severity of the disease is variable.
Stéphanie Pannier +1 more
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Joint pain in hereditary multiple exostoses [PDF]
BMJ, 2015 A 72 year old man who had never undergone joint surgery was referred to an orthopaedic clinic because of pain and stiffness in his right hip, which had been gradually worsening for many years. He was known to have hereditary multiple exostoses but was otherwise well. He had not noticed any recent new bony lumps. Pelvic radiography was performed (fig 1⇓)
David Bruce +2 more
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Orthopaedics and Trauma, 2009
Abstract Multiple hereditary exostoses is an autosomal dominant condition with a prevalence of 1:50, 000. Orthopaedic manifestations are of deformity and compression syndromes. In this article, the genetics, clinical presentation and orthopaedic management are discussed.
Payam Tarassoli +5 more
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Abstract Multiple hereditary exostoses is an autosomal dominant condition with a prevalence of 1:50, 000. Orthopaedic manifestations are of deformity and compression syndromes. In this article, the genetics, clinical presentation and orthopaedic management are discussed.
Payam Tarassoli +5 more
openaire +2 more sources
Hereditary Multiple Exostoses With Myelopathy
Archives of Neurology, 1979A 58-year-old woman with hereditary multiple exostoses had slowly progressive myelopathy due to a vertebral exostosis that compressed the spinal cord at T1-2. She did not show skeletal deformities, but had numerous palpable long-bone exostoses. While CNS complications are rare in hereditary multiple exostosis, 17 other cases have been reported.
Howard L. Lipton, Sam U. Ho
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Clinical Orthopaedics and Related Research, 1984
In a family with hereditary multiple exostoses (diaphyseal aclasis), six generations are known to have been affected. Thirty-three of 85 family members have had the disorder. This condition affects the long bones, pelvis, scapulae, and ribs, and the exostoses continue to enlarge until epiphyseal fusion occurs.
L L Field +3 more
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In a family with hereditary multiple exostoses (diaphyseal aclasis), six generations are known to have been affected. Thirty-three of 85 family members have had the disorder. This condition affects the long bones, pelvis, scapulae, and ribs, and the exostoses continue to enlarge until epiphyseal fusion occurs.
L L Field +3 more
openaire +3 more sources
Scoliosis in patients with multiple hereditary exostoses
European Spine Journal, 2015To investigate the prevalence of and to identify independent predictors associated with scoliosis in patients with multiple hereditary exostoses (MHE).Fifty patients with MHE were clinically examined, and the diagnosis of scoliosis was made based on radiographs.
Kazu Matsumoto +5 more
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