Literature DB >> 6941778

Bile acid metabolism in mild arteriohepatic dysplasia.

D M Collins, F T Shannon, C B Campbell.   

Abstract

Arteriohepatic dysplasia is a rare congenital syndrome in which attenuated peripheral pulmonary arteries are associated with liver impairment. The earliest indication is usually persistent cholestatic jaundice in the first few months after birth. Although this is invariably associated with pruritus, bile acid kinetic studies have not been reported in such patients. This report describes a girl with a particularly mild form of the syndrome who was never observed to be clinically or biochemically jaundiced. Bile acid studies indicated that there was a defect in bile acid excretion but not in uptake or conjugation.

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Year:  1981        PMID: 6941778     DOI: 10.1111/j.1445-5994.1981.tb03735.x

Source DB:  PubMed          Journal:  Aust N Z J Med        ISSN: 0004-8291


  4 in total

Review 1.  The Alagille syndrome (arteriohepatic dysplasia).

Authors:  R F Mueller
Journal:  J Med Genet       Date:  1987-10       Impact factor: 6.318

2.  Investigation of serum bile acids; seven patients with Alagille syndrome.

Authors:  K Obinata; N Nakatsu; T Watanabe; S Niijima; O Arisaka; H Sasaki; H Nittono; K Yabuta; T Miyano
Journal:  Eur J Pediatr       Date:  1985-09       Impact factor: 3.183

3.  Biliary lipid metabolism in children with chronic intrahepatic cholestasis.

Authors:  M Becker; K von Bergmann; H W Rotthauwe; O Leiss
Journal:  Eur J Pediatr       Date:  1984-11       Impact factor: 3.183

4.  Effects of phenobarbital on biliary lipid metabolism in children with chronic intrahepatic cholestasis.

Authors:  M Becker; K von Bergmann; H W Rotthauwe; O Leiss
Journal:  Eur J Pediatr       Date:  1984-11       Impact factor: 3.183

  4 in total

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