Hereditary multiple exostosis : a study in abnormal bone growth [PDF]
, 2020 Hereditary multiple exostosis is a generalised, heritable disorder of bone, characterised by the appearance of numerous cartilagecappecl exostoses at the juxta-epiphysial regions of the endochondral skeleton.
Solomon, Louis
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Hereditary multiple exostoses (HME) [PDF]
, 2000 Review on Hereditary multiple exostoses (HME), with data on clinics, and the genes ...
Bovée, JVMG
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Radiological conference. Osteopoikilosis [PDF]
, 1998 published_or_final_versio
Peh, WCG, Wong, LLS
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Solitary Osteochondroma Arising from Cervical Spina Bifida Occulta [PDF]
, 2013 Solitary osteochondromas are common benign long bone tumors originating from cartilage. They may produce a wide variety of symptoms and complications depending on their spinal location.
Abdallah, Anas +2 more
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Osteochondroma and multiple cartilagenous exostosis involving the distal radius and ulna on adjacent cortices : an unusual manifestation of a common condition [PDF]
, 2014 The findings of two canine patients presenting with distal antebrachial multiple cartilaginous exostoses (MCE) highlights the difference in presentation and clinical significance of MCE impinging on the adjacent radius and ulna.
Bogner, Gary +2 more
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Growth modulation in genu valgum secondary to multiple hereditary exostosis [PDF]
Hereditary Multiple Exostoses (HME) is a rare disease with a prevalence of 1:50,000, which can manifest in various ways. This cartilaginous tumor can appear in a spectrum, ranging from mobility restriction to chronic pain and alignment disorders ...
Ismail, Imma Isniza +2 more
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Correction and lengthening for deformities of the forearm in multiple cartilaginous exostoses [PDF]
, 2006 金沢大学医学部附属病院整形外科Background. Multiple cartilaginous exostoses cause various deformities of the epiphysis. In exostoses of the ulna, the ulna is shortened and the radius acquires varus deformity, which may lead to dislocation of the radial head.
Matsubara Hidenori +5 more
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Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11. [PDF]
, 1996 A contiguous gene syndrome due to deletions of the proximal short arm of chromosome 11 is described in eight patients belonging to four families. The main clinical features are multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and ...
Bartsch, Oliver +11 more
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Imaging of Primary and Recurrent Tumours
, 2002 Sarcoma, Volume 6, Issue S1, Page S25-S28, 2002.
wiley +1 more source