2005
DOI: 10.1111/j.1365-2265.2005.02330.x
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The role of growth hormone in determining birth size and early postnatal growth, using congenital growth hormone deficiency (GHD) as a model

Abstract: Length, weight and BMI data from our study groups suggest that GH per se has a minimal effect on intrauterine growth but a significant effect during the infancy period. Early growth may also be influenced by the complexity of the hypopituitary phenotype reflected by the presence of additional pituitary hormone deficiencies and midline forebrain defects.

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Cited by 56 publications
(47 citation statements)
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“…In human cord blood, the insulin level is correlated with birth weight and neonatal length, but not with growth hormone level (21). Conversely, growth hormone has a predominant role in the postnatal period (10), and a study of children with congenital growth hormone deficiency (22) provides evidence that growth hormone has a minimal effect on intrauterine growth but a significant effect during infancy. Our findings, in contrast, suggest that adiponectin has an effect on fetal growth, but no effect on early postnatal growth, at least in the first month of life.…”
Section: Discussionmentioning
confidence: 99%
“…In human cord blood, the insulin level is correlated with birth weight and neonatal length, but not with growth hormone level (21). Conversely, growth hormone has a predominant role in the postnatal period (10), and a study of children with congenital growth hormone deficiency (22) provides evidence that growth hormone has a minimal effect on intrauterine growth but a significant effect during infancy. Our findings, in contrast, suggest that adiponectin has an effect on fetal growth, but no effect on early postnatal growth, at least in the first month of life.…”
Section: Discussionmentioning
confidence: 99%
“…Infant growth is largely a continuation of in utero growth, is influenced predominantly by nutrition, and is largely growth hormone independent (12). Growth during childhood is largely growth hormone dependent (13), although it follows the same final pathway as uterine growth, namely insulin-like growth factor-1, and is evident mathematically from approximately 6 to 8 mo of postnatal life.…”
mentioning
confidence: 99%
“…Clinical findings may become evident in asymptomatic patients with time. Observation is required in the neonatal period for optic nerve hypoplasia, midline defects or u n c o r r e c t e d p r o o f syndromes, even though initial endocrinal evaluations are normal (17)(18)(19). Diagnosis is difficult due to the problems faced with premature infants, hypothalamus-pituitary axis immaturity, limited information on normal values for newborns and contraindicated stimulation tests.…”
Section: Neonatal Clinical Findings In Congenital Hypopituitarism Casesmentioning
confidence: 99%