A child that presents with an acute limp: Legg-Calvé-Perthes disease
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چکیده
منابع مشابه
A child that presents with an acute limp: Legg-Calvé-Perthes disease
A 6-year-old boy presented with the recent development of a right sided limp. He had no known medical conditions. On examination, the patient had limited internal/external rotation and abduction of the right hip. He walked with a non-antalgic gait and was noted to have a positive Trendelenberg sign. Lower extremity radiographs (A) revealed flattening of the right proximal femoral epiphysis with...
متن کاملLegg-Calvé-Perthes disease in a child with osteopetrosis
Osteopetrosis is a rare inherited disorder of bone causing increased bone density. Legg-Calvé-Perthes disease (LCPD), by contrast, is a more common idiopathic condition leading to variable avascular necrosis of the immature femoral head. We present a case of a 5-year-old boy presenting with these co-morbidities. We have found only one previous reference suggesting these two conditions can coexi...
متن کاملLegg-Calvé-Perthes disease: an overview with recent literature.
The evolving knowledge on Legg-Calvé-Perthes (LCP) demonstrates the utility of studying a rare disease systematically by piecing together the biology and mechanics of this condition and applying clinical observations to improve patient care. As treatments of less common diseases are hard to randomize and study in meaningful numbers, long-term study groups have been created to provide insight in...
متن کاملEditorial LEGG - CALVÉ - PERTHES DISEASE : 100 YEARS
Legg-Calvé-Perthes disease (LCPD) started to be studied 100 years ago (1910), thanks to the advent of the possibility of conducting clinical studies by means of radiographic images (1895). However, many questions remain open, both in relation to the etiology of this orthopedic condition and in relation to which therapeutic measures are valid. Thus, great controversy has been generated. In 1910,...
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ژورنال
عنوان ژورنال: Pan African Medical Journal
سال: 2016
ISSN: 1937-8688
DOI: 10.11604/pamj.2016.23.51.8871