PDF-rarechromoorg

Author : catherine | Published Date : 2021-09-15

NONOassociatedXlinked ID syndromeRare Chromosome Disorder Support Group Charity Number 1110661Registered in England and Wales Company Number 546041

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rarechromoorg: Transcript

NONOassociatedXlinked ID syndromeRare Chromosome Disorder Support Group Charity Number 1110661Registered in England and Wales Company Number 546041. 1712 microdulications217q12 microduplicationsA 17q12 microduplication is a rare genetic condition caused by a tiny extra art of one of the bodys 46 chromosomes chromosome 17 For healthy development c Phelan-McDermid syndrome 2213 deletions 2Phelan-McDermid syndrome 22q13 deletionsA 22q13 deletion means that the cells of the body have a small but variable amount of genetic material missing from one Small Supernumerary Marker Chromosomes (sSMC) 2 Small supernumerary marker chromosomes This leaflet tells you what we know about the estimated 3.5 million people in the world who have a small super

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