The Epidemiology and Demographics of Legg-Calvé-Perthes' Disease
Author(s) -
Randall T. Loder,
Elaine N. Skopelja
Publication year - 2011
Publication title -
isrn orthopedics
Language(s) - English
Resource type - Journals
eISSN - 2090-617X
pISSN - 2090-6161
DOI - 10.5402/2011/504393
Subject(s) - medicine , legg calve perthes disease , incidence (geometry) , pediatrics , epidemiology , etiology , disease , demographics , hypophosphatasia , demography , biochemistry , chemistry , physics , alkaline phosphatase , sociology , optics , enzyme
The etiology of Legg-Calvé-Perthes' disease (LCPD) is unknown. There are many insights however from epidemiologic/demographic information. A systematic medical literature review regarding LCPD was performed. The incidence ranges from 0.4/100,000 to 29.0/100,000 children <15 years of age. There is significant variability in incidence within racial groups and is frequently higher in lower socioeconomic classes. The typical age at presentation ranges from 4 to 8 years (average 6.5 years), except for children from the Indian subcontinent (average 9.5 years). There is a mild familial component. The children demonstrate impaired growth in height, skeletal age, and birth weight. This impaired growth coincides with an age appropriate reduced somatomedin A activity and decreased levels of IGF. LCPD can be associated with abnormalities in the coagulation cascade, including an increase in factor V Leiden mutation, low levels of protein C and/or S, and decreased antithrombin activity. There is decreased turnover in type I collagen and synthesis of type III collagen, as well as reduced levels of urinary glycosaminoglycans in the active phases of the disorder. Subtle abnormalities in the opposite hip and other minor/major congenital defects are reported. Children with LCPD are active and score abnormally in certain standardized psychological tests.
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