Results 131 to 140 of about 3,566 (172)

Hereditary Multiple Exostoses with Pseudoaneurysm

CardioVascular and Interventional Radiology, 2007
A 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
Azmy M, Al-Hadidy, Moa'ath M, Al-Smady, Azmi A, Haroun, Hanan A, Hamamy, Suha M, Ghoul, Akram O, Shennak   +5 more
openaire   +2 more sources

The hip in hereditary multiple exostoses

The Journal of Bone and Joint Surgery. British volume, 2001
We defined the characteristics of dysplasia and coxa valga in hereditary multiple exostoses (HME) by radiological analysis of 24 hips in 12 patients. The degree and effect of the ‘osteochondroma load’ around the hip were quantified. We investigated the pathology of the labrum and the incidence of osteoarthritis and of malignant change in these ...
D E, Porter, M K, Benson, G A, Hosney
openaire   +2 more sources

Manifestations of Hereditary Multiple Exostoses

Journal of the American Academy of Orthopaedic Surgeons, 2005
The solitary osteochondroma, a common pediatric bone tumor, is a cartilage-capped exostosis. Hereditary multiple exostosis is an autosomal dominant disorder manifested by the presence of multiple osteochondromas. Linkage analysis has implicated mutations in the EXT gene family, resulting in an error in the regulation of normal chondrocyte proliferation
Jonathan R, Stieber, John P, Dormans
openaire   +2 more sources

Multiple Cartilaginous Exostoses in the Dog

Journal of the American Veterinary Medical Association, 1975
SUMMARY The clinicopathologic aspects of multiple cartilaginous exostoses (mce) in 2 dogs were compared with those in 9 previously reported cases of mce in dogs. Although a familial tendency is probable, there is apparently no sex or breed predilection. Only bones that developed by endochondral ossification were affected.
P C, Gambardella, C A, Osborne, J B, Stevens   +2 more
openaire   +2 more sources

Hereditary Multiple Exostoses With Myelopathy

Archives of Neurology, 1979
A 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.
S U, Ho, H L, Lipton
openaire   +2 more sources

Hereditary Multiple Exostoses

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.
B F, Crandall, L L, Field, R S, Sparkes, M A, Spence   +3 more
openaire   +2 more sources

Multiple cartilaginous exostoses in a dog

Journal of Small Animal Practice, 1981
ABSTRACTA case of multiple cartilaginous exostoses (osteochondromatosis) in a 9‐month‐old Kelpie cross dog is described. This uncommon dyschondroplasia, which resembled multiple cartilaginous exostoses in man, involved the radius, the femur, a metacarpal and metatarsal bone, the phalanges of three extremities, the pelvis, the ribs and cervical ...
J W, Finnie, I R, Sinclair
openaire   +2 more sources

Hereditary multiple exostoses and enchondromatosis

Best Practice & Research Clinical Rheumatology, 2008
Hereditary 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, Laurence, Legeai-Mallet   +1 more
openaire   +2 more sources

Multiple hereditary exostoses and enchondromatosis

Best Practice & Research Clinical Rheumatology, 2020
Multiple 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.
openaire   +2 more sources

[Multiple exostoses].

Nihon rinsho. Japanese journal of clinical medicine, 2000
Multiple exostoses is a hereditary disease characterized by multiple osteocartilagenous tumors, of which the histological structures are similar to those of normal epiphyses. Genetic linkage has identified three different loci for this disease: EXT1 on 8q, EXT2 on 11p, and EXT3 on 19p.
J, Toguchida, S, Nagayama
openaire   +1 more source