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The presence of obesity in at least one parent significantly increases the risk that an obese child will become an obese adult.
While there are genetic conditions which predispose or even cause children and adolescents to become overweight or obese, it is usually not the primary reason for weight problems in this country. In fact, only a small percentage of childhood obesity is associated with a hormonal or genetic defect. Children, like adults, mostly gain weight when energy input (food) exceeds energy output (exercise).
Interestingly, studies have shown that on average, some overweight or obese children do not consume significantly more calories (food) than their thin similarly aged counterparts. In simplistic terms, it is not that they are eating more, but rather doing fewer activities. This leads to a positive energy state in the body, which will result in weight gain.
So a relatively small imbalance between caloric intake and energy or physical output can lead to significant weight gain over time. This is what is scene, with most obese children demonstrating a slow but consistent weight gain over several years. Fortunately, diet and physical activity are susceptible to behavior modification, and the first step is weight awareness.
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Examples of Genetic Causes of Childhood Obesity |
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Hormonal causes |
Diagnostic clues |
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Hypothyroidism |
Increased TSH*, decreased thyroxine (T4) levels |
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Hypercortisolism |
Abnormal dexamethasone suppression test; increased 24-hour free urinary cortisol level |
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Primary hyperinsulinism |
Increased plasma insulin, increased C-peptide levels |
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Pseudohypoparathyroidism |
Hypocalcemia, hyperphosphatemia, increased PTH* level |
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Acquired hypothalamic |
Presence of hypothalamic tumor, infection, syndrome trauma, vascular lesion |
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Genetic syndromes |
Associated characteristics |
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Prader-Willi |
Obesity, unsatiable appetite, mental retardation, hypogonadism, strabismus |
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Laurence-Moon/Bardet-Biedl |
Obesity, mental retardation, pigmentary retinopathy, hypogonadism, spastic paraplegia |
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Alström |
Obesity, retinitis pigmentosa, deafness, diabetes mellitus |
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Börjeson-Forssman-Lehmann |
Obesity, mental retardation, hypogonadism, hypometabolism, epilepsy |
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Cohen |
Truncal obesity, mental retardation, hypotonia, hypogonadism |
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Turner's |
Short stature, undifferentiated gonads, cardiac abnormalities, webbed neck, obesity, 45, X genotype |
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Familial lipodystrophy |
Muscular hypertrophy, acromegalic appearance, liver enlargement, acanthosis nigricans, insulin resistance, hypertriglyceridemia, mental retardation |
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Beckwith-Wiedemann |
Gigantism, exomphalos, macroglossia, visceromegaly |
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Sotos' |
Cerebral gigantism, physical overgrowth, hypotonia, delayed motor and cognitive development |
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Weaver |
Infant overgrowth syndrome, accelerated skeletal maturation, unusual facies |
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Ruvalcaba |
Mental retardation, microcephaly, skeletal abnormalities, hypogonadism, brachymetapody |
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Gene associations |
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Leptin |
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Beta3-adrenergic receptor |
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*TSH=thyroid-stimulating hormone; *PTH=parathyroid hormone. |
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