Article Text

Download PDFPDF
Microcephaly-cardiomyopathy: a new autosomal recessive phenotype?
  1. I M Winship,
  2. D L Viljoen,
  3. P M Leary,
  4. M M De Moor
  1. Department of Human Genetics, University of Cape Town Medical School, Observatory, South Africa.

    Abstract

    A distinctive phenotype of severe microcephaly and self-limiting dilated cardiomyopathy has been observed in two sibs suggesting autosomal recessive inheritance. Mental retardation, delayed developmental milestones, and minor dysmorphism were additional features.

    Statistics from Altmetric.com

    Request Permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

    Linked Articles