Layer P, Balzer K, Goebell H
Hepatogastroenterology. 1985 Feb;32(1):31-3.
A West German family with hereditary pancreatitis is described. Four members are definitely known to have had pancreatitis, while three additional members are suspected of having the disease. The mean age of onset of symptoms was 14 years. Known causes of secondary pancreatitis and amino aciduria were ruled out in each case. HLA-segregation was analysed on the A, B, C, and DR loci in all members of the family, but no coupling between distribution of HLA haplotypes and incidence of pancreatitis was detected.
本文描述了一个患有遗传性胰腺炎的西德家庭。明确已知有四名家庭成员患有胰腺炎,另有三名家庭成员疑似患有该病。症状出现的平均年龄为14岁。在每个病例中都排除了继发性胰腺炎和氨基酸尿的已知病因。对该家庭所有成员的A、B、C和DR位点进行了HLA分型分析,但未检测到HLA单倍型分布与胰腺炎发病率之间的关联。