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Phelan McDermid: Difference between revisions
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(PMS) 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> | (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] | [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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[[nl:Syndroom van Phelan-McDermid]] | |||