Acrocallosal Syndrome: A Rare Case Report

Journal Title: Scholars Journal of Medical Case Reports - Year 2017, Vol 5, Issue 3

Abstract

Abstract: Acrocallosal syndrome (ACS) is a very rare genetic disorder characterised by craniofacial malformation in the form of partial or complete agenesis of corpus callosum and different forms of facial, digital abnormality along with moderate to severe mental retardation. It is generally inherited as autosomal recessive disorder and both sex can be affected equally. Diagnosis is mainly by clinical criteria with neuroimaging. Management by only supportive care. Here we present such a rare case. Keywords: Acrocallosal syndrome, corpus callosum agenesis, craniofacial malformation.

Authors and Affiliations

Tapan Kumar Biswas, Sunil Kumar Agarwalla, Shantanu Kumar Meher, Subhranshu Sekhar Dhal

Keywords

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  • EP ID EP379495
  • DOI -
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How To Cite

Tapan Kumar Biswas, Sunil Kumar Agarwalla, Shantanu Kumar Meher, Subhranshu Sekhar Dhal (2017). Acrocallosal Syndrome: A Rare Case Report. Scholars Journal of Medical Case Reports, 5(3), 148-150. https://europub.co.uk/articles/-A-379495