Faecal excretion of alpha-1-antitrypsin in acute diarrhoea.

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Faecal excretion of alpha-1-antitrypsin in acute diarrhoea.

High levels of faecal alpha-1-antitrypsin were found in children suffering from acute rotavirus diarrhoea and in children with diarrhoea in whom no microbial pathogen could be established. The results suggest that transient protein-losing enteropathy is common in acute childhood diarrhoea and may influence the outcome of the disease.

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Faecal alpha-1-antitrypsin and 51Cr-albumin losses in 42 patients with either gastrointestinal or hepatic disease were compared. The reference range was derived from measurements in 20 controls without gastrointestinal disease. Alpha-1-antitrypsin excretion was increased in patients with excessive 51Cr-albumin loss, and correlations were found between alpha-1-antitrypsin clearance and 51Cr-albu...

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Faecal alpha-1-antitrypsin and excretion of 111indium granulocytes in assessment of disease activity in chronic inflammatory bowel diseases.

Intestinal protein loss in chronic inflammatory bowel diseases may be easily determined by measurement of alpha-1-antitrypsin (alpha 1-AT) stool concentration and alpha 1-AT clearance. Both parameters were significantly raised in 36 and 34 patients respectively with chronic inflammatory bowel diseases, compared with eight patients with non-inflammatory bowel diseases, or 19 healthy volunteers. ...

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Alpha- 1 Antitrypsin Deficiency in Children: Pulmonary Involvement

Introduction: α1-antitrypsin deficiency (α1-ATD) is one of the most common genetic disorders in white race, a usual cause of liver disease in children, and hepatopulmonary involvement in children and adult. The aim of this case description is presenting a child with early lung disease without liver parenchymal disorder. Case presentation: We describe a 13 year old boy because of exertional dysp...

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Alpha-1 antitrypsin deficiency is an inherited disorder that may cause severe lung and liver disease.

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood

سال: 1982

ISSN: 0003-9888,1468-2044

DOI: 10.1136/adc.57.2.154