Neuropediatrics 1975; 6(2): 210-219
DOI: 10.1055/s-0028-1091664
Case report

© 1975 by Thieme Medical Publishers, Inc.

Kindred with a Hereditary Caudal Malformation Syndrome

P. de Château, O. Finnström, F. Probst
  • Department of Paediatrics, Umea University, Umea, Department of Paediatrics Linköping University, Linköping and Department of Diagnostic Radiology II, Umea University, Umea/Sweden
Further Information

Publication History

1974

1975

Publication Date:
18 November 2008 (online)

A kindred with a hereditary caudal malformation syndrome is reported. The hereditary trait, as shown in a pedigree, is probably dominant autosomal, with variable expressivity. The presenting symptoms and signs, and the diagnostic procedures are discussed in some detail from a practical point of view. Attention is also paid to the theoretical aspects of etiology and pathogenesis.