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[[nl:Syndroom van Phelan-McDermid]]

Revision as of 18:49, 24 September 2018

(PMS[1]) is a rare genetic condition caused by deletion of terminal end of chromosome 22[2] , about 44% of people develops seizures[3]

Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome

  1. https://www.ncbi.nlm.nih.gov/books/NBK1198/
  2. Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology
  3. DMSF