Calcium Metabolism in Idiopathic Hypercalcaemia of Infancy with Failure to Thrive

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Calcium metabolism in idiopathic hypercalcaemia of infancy with failure to thrive.

As pointed out by a leader in the Lancet (1953), marasmus or 'teething' no longer satisfies paediatricians as a diagnosis for an infant's failure to thrive. The clinical studies of Lightwood and the biochemical work of Payne have recently shown that failure to thrive with constipation, hypotonia, polyuria, loss of appetite with occasional vomiting and intermittent urinary infection may be assoc...

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Biochemical studies in idiopathic hypercalcaemia of infancy.

Idiopathic hypercalcaemia tends to develop between the first and fifteenth months of life and diagnosis rests primarily on biochemical findings. We have determined for this age period the normal values for serum calcium, serum cholesterol and the serum cholesterol fractions by the methods which we use. Over a period of four years samples of blood were taken from 110 infants in hospital, or atte...

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Failure to THRIVE.

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Failure to thrive.

1 Sponsor Disclosure: Financial support for this presentation was provided by Nestlé HealthCare Nutrition, Inc. The views expressed herein are those of the presenter and do not necessarily represent Nestlé’s views. The material herein is accurate as of the date it was presented and is for educational purposes only and is not intended as a substitute for medical advice. Reproduction or distribut...

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The Prevalence of Celiac Disease in Children with Unexplained Failure to Thrive in South West of Iran

Background Celiac disease (CD), considered as a common chronic and genetic diseases that caused by hypersensitivity to gluten. Failure to thrive (FTT), is one of three major clinical features of CD during childhood. The current study aimed to determine the prevalence of celiac disease in children with unexplained FTT in South West of Iran. Materials and Methods  This cross‑sectional study was ...

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood

سال: 1955

ISSN: 0003-9888,1468-2044

DOI: 10.1136/adc.30.153.399