Review began 04/14/2022 review ended 05/16/2022 published 05/18/2022 © copyright

HIGHLIGHTS

  • who: Report and collaborators from the (UNIVERSITY) have published the paper: Review began 04/14/2022 Review ended 05/16/2022 Published 05/18/2022 u00a9 Copyright, in the Journal: (JOURNAL) of May/18,/2022
  • what: Being a rare condition, MCAP requires careful clinical evaluation and neuroimaging for its diagnosis.

SUMMARY

    Megalencephaly-capillary malformation-polymicrogyria syndrome (MCAP) is an uncommon genetic syndrome characterized by primary megalencephaly, cutaneous vascular malformations, polymicrogyria, and other anomalies. In 2007, this condition was renamed macrocephaly-capillary malformation syndrome (MCM) by Toriello and Mulliken et_al and Conway . . .

     

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