View source for Phelan McDermid

(PMS<ref>https://www.ncbi.nlm.nih.gov/books/NBK1198/</ref>) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology</ref> , about 44% of people develops [[epilepsy|seizures]]<ref>DMSF</ref>

[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/pdf/fnsyn-10-00011.pdf Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome]

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