Fig. 1From: Novel GLI3 variant causing overlapped Greig cephalopolysyndactyly syndrome (GCPS) and Pallister-Hall syndrome (PHS) phenotype with agenesis of gallbladder and pancreasMacroscopic findings at autopsy. The stillborn had a proportionally unbalanced, large head with acrocephaly (a). Postaxial polysyndactyly of the right hand was noted (b) and (c, photography by soft X-ray). While the shape and size of the liver were normal, the gallbladder was nonexistent at the hepatic portal section (d, hatched area). Hypoplasia of both kidneys (e) was noted (arrows)Back to article page