Hunter A G, Jimenez C, Tawagi F G
Division of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada.
Am J Med Genet. 1991 Nov 1;41(2):201-7. doi: 10.1002/ajmg.1320410214.
Ivemark et al. first described sibs with renal-hepatic-pancreatic dysplasia (RHPD) (Ivemark BI, Oldfelt V, Zetterström R (1959): Acta Pediatr Scand 48: 1-11). Subsequent reports of affected individuals have described additional malformations and syndromes associated with RHPD. In this paper we describe 2 sibs with RHPD in association with Dandy-Walker cyst (DW). Through an examination of the pattern of associated malformations seen in RHPD we argue that RHPD-DW is a distinct monogenetic syndrome, and not an association.
伊韦马克等人首次描述了患有肾-肝-胰发育不良(RHPD)的同胞(伊韦马克BI、奥尔德费尔特V、泽特斯特伦R(1959年):《儿科学报》48:1 - 11)。随后关于受累个体的报告描述了与RHPD相关的其他畸形和综合征。在本文中,我们描述了2例患有RHPD并伴有丹迪-沃克囊肿(DW)的同胞。通过对RHPD中所见相关畸形模式的研究,我们认为RHPD - DW是一种独特的单基因综合征,而非一种关联。