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<a href="http://doi.org/10.1097/01.mph.0000165138.60991.mL" target="_blank" rel="noreferrer noopener">http://doi.org/10.1097/01.mph.0000165138.60991.mL</a>
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Pages
440-444
Issue
4
Volume
25
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Title
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Increased chondrocyte apoptosis in growth plates from children with slipped capital femoral epiphysis
Publisher
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Journal of Pediatric Orthopaedics
Date
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2005
2005-07
Subject
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apoptosis; Orthopedics; pathogenesis; Pediatrics; programmed cell-death; slipped capital femoral epiphysis; terminal hypertrophic chondrocytes
Creator
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Adamczyk M J; Weiner D S; Nugent A; McBurney D; Horton W E
Description
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Ultrastructural studies of slipped capital femoral epiphysis (SCFE) growth plates have shown diminished cellularity and marked distortion of the architecture in the proliferative and hypertrophic zones. Chondrocyte degeneration and death were noted at all levels of the hypertrophic and proliferative zones, suggesting an accelerated disturbance in the life-to-death cycle of the chondrocytes. The current study examines the mechanism responsible for the diminished cell number and whether increased programmed cell death (apoptosis) or necrosis was operative. proximal femoral growth plates from patients with SCFE (three patients) were prepared and sectioned for histochemistry, in situ detection of apoptosis, and immunohistochemistry. The results showed that the diminished cell number is due to an abnormal frequency and distribution of chondrocytes undergoing apoptosis. Although it is unclear whether the increased apoptosis is occurring early or late in the disease, it is highly likely that it is directly linked to pathogenesis.
Identifier
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<a href="http://doi.org/10.1097/01.mph.0000165138.60991.mL" target="_blank" rel="noreferrer noopener">10.1097/01.mph.0000165138.60991.mL</a>
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Journal Article or Conference Abstract Publication
2005
Adamczyk M J
Apoptosis
Horton W E
Journal Article or Conference Abstract Publication
Journal of Pediatric Orthopaedics
McBurney D
Nugent A
Orthopedics
Pathogenesis
Pediatrics
programmed cell-death
slipped capital femoral epiphysis
terminal hypertrophic chondrocytes
Weiner D S