Article Text

Download PDFPDF
Rare disease
Acrocallosal syndrome in a young hypertensive male
  1. Vishal V Ramteke,
  2. Pramod A Darole,
  3. Zohaib Farooqui Shaikh,
  4. Namita J Padwal,
  5. Brijesh Agrawal,
  6. Makardhwaj S Shrivastava,
  7. Sandhya Kamath
  1. Department of Medicine, Lokmanya Tilak Municipal Medical College and General Hospital, Mumbai, India
  1. Correspondence to Dr Makardhwaj Sarvadaman Shrivastava, makar_in{at}rediffmail.com

Summary

Acrocallosal syndrome is an extremely rare genetic disorder with autosomal recessive inheritance. It is characterised by moderate to severe mental retardation, hypotonia, agenesis of the corpus callosum and preaxial polydactyly involving both feet and the facial features like broad forehead and hypertelorism. The authors report a case of a young hypertensive male who presented with unprovoked seizures for the first time who had multiple craniofacial, digital dysmorphic features with moderate mental retardation. The diagnosis of acrocallosal syndrome was arrived at after neuroimaging showed agenesis of corpus callosum with interhemispheric cysts.

View Full Text

Statistics from Altmetric.com

Footnotes

  • Competing interests None.

  • Patient consent Obtained.

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.