Prenatal diagnosis of MPPH syndrome

Prenat Diagn. 2013 Mar;33(3):292-5. doi: 10.1002/pd.4039. Epub 2013 Jan 24.

Abstract

We report the prenatal sonographic detection of a fetus with megalencephaly, polymicrogyria, postaxial polydactyly and hydrocephaly. Only 14 patients have been reported in the literature so far, all but one were diagnosed postnatally. The polymicrogyria in the frontoparietal lobe was confirmed by prenatal magnetic resonance imaging. Additionally, a hypoplastic thymus as seen in a 22q11 deletion was present. Although polymicrogyria along with pre-axial polydactyly has been described in 22q11 deletion, the diagnosis of Di George syndrome was ruled out. The etiology of megalencephaly, polymicrogyria, postaxial polydactyly and hydrocephaly has not been revealed yet. A dominant as well as recessive inheritance has been suggested.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Humans
  • Hydrocephalus / diagnosis*
  • Hydrocephalus / diagnostic imaging
  • Magnetic Resonance Imaging
  • Malformations of Cortical Development / diagnosis*
  • Malformations of Cortical Development / diagnostic imaging
  • Polydactyly / diagnosis*
  • Polydactyly / diagnostic imaging
  • Pregnancy
  • Prenatal Diagnosis
  • Ultrasonography

Supplementary concepts

  • Megalancephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome