Brain computer tomography cuts of the patient, demonstrating basal ganglia and periventricular calcification. From a case report by Tonelli et al., 2007
Tonelli AR, Kosuri K, Wei S, Chick D (2007). "Seizures as the first manifestation of chromosome 22q11.2 deletion syndrome in a 40-year old man: a case report". J Med Case Reports. 1: 167. doi:10.1186/1752-1947-1-167. PMC2222674. PMID 18053182.CS1 maint: multiple names: authors list (link)
Muldoon M, Ousley OY, Kobrynski LJ, Patel S, Oster ME, Fernandez-Carriba S, Cubells JF, Coleman K, Pearce BD (September 2015). "The effect of hypocalcemia in early childhood on autism-related social and communication skills in patients with 22q11 deletion syndrome". Eur Arch Psychiatry Clin Neurosci. 265 (6): 519–24. doi:10.1007/s00406-014-0546-0. PMC4379129. PMID 25267002.
Zinkstok J, van Amelsvoort T (2005). "Neuropsychological profile and neuroimaging in patients with 22Q11.2 Deletion Syndrome: a review". Child Neuropsychol. 11 (1): 21–37. doi:10.1080/09297040590911194. PMID 15823981.
กล, มอาการด, จอร, งกฤษ, digeorge, syndrome, หร, อกล, มอาการการหล, ดหายของตำแหน, 22q11, งกฤษ, 22q11, deletion, syndrome, เก, ดจากการหล, ดหายของส, วนหน, งของโครโมโซม, อเป, นโรคในกล, มของกล, มอาการไมโครด, การหล, ดหายขนาดเล, พบบ, อยท, โดยเก, ดข, นท, ตำแหน, 22q11, . klumxakardicxrc xngkvs DiGeorge syndrome hruxklumxakarkarhludhaykhxngtaaehnng 22q11 xngkvs 22q11 deletion syndrome ekidcakkarhludhaykhxngswnhnungkhxngokhromosm 22 thuxepnorkhinklumkhxngklumxakarimokhrdilichn karhludhaykhnadelk thiphbbxythisud odyekidkhunthitaaehnng 22q11 2 thaythxdaebbxxotosmlksnaedn inkhwamchukxyuthipraman 1 4000 phawaniidrbkarbrryayiwkhrngaerkemux kh s 1968 odykumaraephthytxmirthx Angelo DiGeorge nxkcakniphawaniyngsmphnthkborkhhwicaetkaenidchnid truncus arteriosus aela Tetralogy of Fallot xikdwy22q11 2 deletion syndromeBrain computer tomography cuts of the patient demonstrating basal ganglia and periventricular calcification From a case report by Tonelli et al 2007 1 bychicaaenkaelalingkipphaynxkICD 10D82 1ICD 9279 11 758 32OMIM188400DiseasesDB3631eMedicinemed 567 ped 589derm 716MeSHD004062GeneReviews22q11 2 Deletion Syndromexakaraelaxakaraesdng aekikhkhwambkphrxngthangkarrbru aekikh phupwyedkklumxakardicxrcmkmiradbstipyyaxyuinchwngkakungrahwangpktikhxnkhangtaaelata aelamkmikhwamsamarththangdankarichkhaphuddikwadanxun bangraysamarthekhaeriyninorngeriynpktiid aetbangraytxngekhaorngeriynkarsuksaphiesshruxeriynthiban khwamrunaerngkhxngphawaaekhlesiymineluxdtainwyedkelkmikhwamsmphnthkbkhwamrunaerngkhxngphvtikrrmkhlayxxthistikinwyotkhun 2 phuihythimiklumxakardicxrccamikhwamesiyngsungthicaekidorkhcitephth schizophrenia ody 30 caekhymixakarkhxngorkhcit psychosis xyangnxyhnungkhrnginchiwit aelapramanhnunginsicapwyorkhcitephth 3 phupwyklumxakardicxrcmioxkasekidorkhpharkinsnchnidepnerw early onset Parkinson s disease makkwakhnthwip karwinicchyxacmikhwamyaklabakenuxngcakyathiichrksaorkhcitephthcamiphlkhangekhiyngthaihekidxakaraebborkhpharkinsnid thaihkarwinicchylachaxxkipidthung 10 pi 4 5 xangxing aekikh Tonelli AR Kosuri K Wei S Chick D 2007 Seizures as the first manifestation of chromosome 22q11 2 deletion syndrome in a 40 year old man a case report J Med Case Reports 1 167 doi 10 1186 1752 1947 1 167 PMC 2222674 PMID 18053182 CS1 maint multiple names authors list link Muldoon M Ousley OY Kobrynski LJ Patel S Oster ME Fernandez Carriba S Cubells JF Coleman K Pearce BD September 2015 The effect of hypocalcemia in early childhood on autism related social and communication skills in patients with 22q11 deletion syndrome Eur Arch Psychiatry Clin Neurosci 265 6 519 24 doi 10 1007 s00406 014 0546 0 PMC 4379129 PMID 25267002 Zinkstok J van Amelsvoort T 2005 Neuropsychological profile and neuroimaging in patients with 22Q11 2 Deletion Syndrome a review Child Neuropsychol 11 1 21 37 doi 10 1080 09297040590911194 PMID 15823981 xangxingphidphlad payrabu lt ref gt imthuktxng immikarkahndkhxkhwamsahrbxangxingchux Butcher 2013 Mok KY Sheerin U Simon Sanchez J Salaka A Chester L Escott Price V aelakhna May 2016 Deletions at 22q11 2 in idiopathic Parkinson s disease a combined analysis of genome wide association data Lancet Neurol 15 6 585 96 doi 10 1016 S1474 4422 16 00071 5 PMC 4828586 PMID 27017469 bthkhwamekiywkbaephthysastrniyngepnokhrng khunsamarthchwywikiphiediyidodyephimkhxmul duephimthi sthaniyxy aephthysastrekhathungcak https th wikipedia org w index php title klumxakardicxrc amp oldid 8110793, wikipedia, วิกิ หนังสือ, หนังสือ, ห้องสมุด,