Abstract
The Prader–Willi Syndrome is characterised by hypotonia in the neonatal period, hypogonadism, short stature, small hands and feet, mental retardation and obesity. However, it is unclear whether the obesity is due primarily to an excessive energy intake, a reduced total energy expenditure or a combination of both these factors (Bray et al, 1983; Coplin et al, 1985). Studies that might contribute knowledge to the question have been hampered by the inability to measure some of the parameters, notably total energy expenditure, especially in children.
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References
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© 1992 Springer-Verlag Berlin Heidelberg
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Davies, P.S.W., Joughin, C., Livingstone, M.B.E., Barnes, N.D. (1992). Energy Expenditure in the Prader-Willi Syndrome. In: Cassidy, S.B. (eds) Prader-Willi Syndrome. NATO ASI Series, vol 61. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-84283-2_21
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DOI: https://doi.org/10.1007/978-3-642-84283-2_21
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