Abstract: | 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. © 1994 Wiley-Liss, Inc. |