Craniofacial anomalies,abnormal hair,camptodactyly, and caudal appendage (Teebi–Shaltout syndrome): Clinical and autopsy findings

Teebi and Shaltout [1989: Am J Med Genet 33: 58–60] described a new syndrome of craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage in children born to a consanguineous couple. We report on a second family with the same pattern of anomalies occurring in a liveborn female and 3 spontaneously aborted fetuses, and include autopsy findings. As additional findings 2 of our cases had unilateral microphthalmia and kidney anomalies. Our observation confirms that this pattern of anomalies is a distinct syndrome with autosomal recessive inheritance; we suggest the synonym Teebi–Shaltout syndrome. © 1993 Wiley-Liss, Inc.