Chrzanowska K, Kozlowski K, Kowalska A
Department of Genetics, Children's Memorial Health Institute, Warsaw, Poland.
Am J Med Genet. 1998 Aug 6;78(5):401-5. doi: 10.1002/(sici)1096-8628(19980806)78:5<401::aid-ajmg1>3.0.co;2-o.
We report on a boy with unique somatic and skeletal manifestations. The syndrome consists of branchial and auricular fistulae, abnormal face, and skeletal abnormalities including foramina parietalia permagna.