Gabrielli O, Carloni I, Catassi C, Natalini G, Coppa G V, Giorgi P
Department of Pediatrics, University of Ancona, Italy.
Am J Med Genet. 1994 Feb 1;49(3):333-6. doi: 10.1002/ajmg.1320490318.
Recently, Stratton and Parker [Am J Med Genet 32:169-173, 1989] reported on a child with a previously undescribed combination of growth hormone deficiency, wormian bones, dextrocardia, brachycamptodactyly, and other midline defects. We report on another patient with similar clinical signs.
最近，斯特拉顿和帕克[《美国医学遗传学杂志》32:169 - 173, 1989]报道了一名儿童，其患有生长激素缺乏、缝间骨、右位心、短指屈曲畸形以及其他中线缺陷的一种此前未描述过的组合情况。我们报道了另一名有类似临床体征的患者。
