Mohan V, Chari S T, Hitman G A, Suresh S, Madanagopalan N, Ramachandran A, Viswanathan M
Diabetes Research Centre, Government Peripheral Hospital, London, U.K.
Pancreas. 1989;4(6):690-3. doi: 10.1097/00006676-198912000-00006.
There is very little information on the genetic factors associated with fibrocalculous pancreatic diabetes (FCPD). Ninety-eight first-degree relatives of FCPD patients were subjected to detailed studies, which included glucose tolerance tests, x-ray films of the abdomen, ultrasonography, and studies of exocrine pancreatic function. The study shows that there is a familial aggregation of FCPD with evidence of vertical transmission of the disease from parent to offspring in some families. Routine screening of families of FCPD probands helped to pick up cases in the stage of impaired glucose tolerance. There is heterogeneity in FCPD with respect to familial factors. Some families show marked familial aggregation of FCPD while in others the disease occurs either sporadically or in association with other family members who have abnormal glucose handling.
关于与纤维钙化性胰腺糖尿病(FCPD)相关的遗传因素的信息非常少。对98名FCPD患者的一级亲属进行了详细研究,包括葡萄糖耐量试验、腹部X光片、超声检查以及外分泌胰腺功能研究。研究表明,FCPD存在家族聚集现象,在一些家庭中有从父母垂直传播至后代的疾病证据。对FCPD先证者的家族进行常规筛查有助于发现糖耐量受损阶段的病例。FCPD在家族因素方面存在异质性。一些家族显示出明显的FCPD家族聚集现象,而在其他家族中,该疾病要么散发出现,要么与其他葡萄糖代谢异常的家庭成员一起出现。