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Stratton-Parker syndrome: confirmation of a new entity
O Gabrielli1, I Carloni, C Catassi
1Department of Pediatrics, University of Ancona, Italy.
American Journal of Medical Genetics
|February 1, 1994
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.