| Literature DB >> 16901451 |
Michel Mittelbronn1, Rudi Beschorner, David Capper, Markus Haist, Richard Meyermann, Matthias Meyer-Wittkopf.
Abstract
As holoprosencephaly and Chiari II malformation differ considerably, both in pathogenesis and in phenotypic localization, the coincidence of both entities is extremely rare. The case presented is, to our knowledge, the first published report comprising a combination of a semilobar holoprosencephaly associated with a Chiari II malformation and a myelomeningocele diagnosed prenatally and confirmed by postmortem neuropathologic evaluation. These findings indicate that in the case of pre- and postnatal detection of a myelomeningocele and/or Chiari II malformation, possible additional intracranial malformation, such as a semilobar holoprosencephaly, should also be taken into account and vice versa.Entities:
Mesh:
Year: 2006 PMID: 16901451 DOI: 10.1177/08830738060210051501
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987