Human monosomy[edit] Human conditions due to monosomy: Turner syndrome – People with Turner syndrome typically have one X chromosome instead of the usual two sex chromosomes. Turner syndrome is the only full monosomy that is seen in humans—all other cases of full monosomy are lethal and the individual will not survive development. Cri du chat syndrome – (French for "cry of the cat" after the distinctive noise by affected persons' malformed larynx) a partial monosomy caused by a deletion of the end of the short p (from the word petit, French for "small") arm of chromosome 5 1p36 deletion syndrome – a partial monosomy caused by a deletion at the end of the short p arm of chromosome 1

See also[edit] Anaphase lag Miscarriage

References[edit] ^ "CRC - Glossary M". Archived from the original on 2007-08-08. Retrieved 2007-12-23.  v t e Chromosome abnormalities (Q90–Q99, 758) Autosomal Trisomies Down syndrome 21 Edwards syndrome 18 Patau syndrome 13 Trisomy 9 Warkany syndrome 2 8 Cat eye syndrome/Trisomy 22 22 Trisomy 16 Monosomies/deletions 1q21.1 deletion syndrome/1q21.1 duplication syndrome/TAR syndrome 1 Wolf–Hirschhorn syndrome 4 Cri du chat/Chromosome 5q deletion syndrome 5 Williams syndrome 7 Jacobsen syndrome 11 Miller–Dieker syndrome/Smith–Magenis syndrome 17 DiGeorge syndrome 22 22q11.2 distal deletion syndrome 22 22q13 deletion syndrome 22 genomic imprinting Angelman syndrome/Prader–Willi syndrome (15) Distal 18q-/Proximal 18q- X/Y linked Monosomy Turner syndrome (45,X) Trisomy/tetrasomy, other karyotypes/mosaics Klinefelter syndrome (47,XXY) XXYY syndrome (48,XXYY) XXXY syndrome (48,XXXY) 49,XXXYY 49,XXXXY Triple X syndrome (47,XXX) Tetrasomy X (48,XXXX) 49,XXXXX Jacobs syndrome (47,XYY) 48,XYYY 49,XYYYY 45,X/46,XY Translocations Leukemia/lymphoma Lymphoid Burkitt's lymphoma t(8 MYC;14 IGH) Follicular lymphoma t(14 IGH;18 BCL2) Mantle cell lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large-cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22 BCR) Acute myeloblastic leukemia with maturation t(8 RUNX1T1;21 RUNX1) Acute promyelocytic leukemia t(15 PML,17 RARA) Acute megakaryoblastic leukemia t(1 RBM15;22 MKL1) Other Ewing's sarcoma t(11 FLI1; 22 EWS) Synovial sarcoma t(x SYT;18 SSX) Dermatofibrosarcoma protuberans t(17 COL1A1;22 PDGFB) Myxoid liposarcoma t(12 DDIT3; 16 FUS) Desmoplastic small-round-cell tumor t(11 WT1; 22 EWS) Alveolar rhabdomyosarcoma t(2 PAX3; 13 FOXO1) t (1 PAX7; 13 FOXO1) Other Fragile X syndrome Uniparental disomy XX male syndrome/46,XX testicular disorders of sex development Marker chromosome Ring chromosome 6; 9; 14; 15; 18; 20; 21, 22 Retrieved from "" Categories: CytogeneticsChromosomal abnormalitiesHidden categories: Infobox medical condition

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Specialty (medicine)Medical GeneticsInternational Statistical Classification Of Diseases And Related Health ProblemsICD-10Medical Subject HeadingsAneuploidyChromosomeTurner SyndromeCri Du ChatLarynxChromosome 51p36 Deletion SyndromeChromosome 1Anaphase LagMiscarriageTemplate:Chromosomal AbnormalitiesTemplate Talk:Chromosomal AbnormalitiesChromosome AbnormalityICD-10 Chapter XVII: Congenital Malformations, Deformations And Chromosomal AbnormalitiesList Of ICD-9 Codes 740–759: Congenital AnomaliesAutosomeTrisomyDown SyndromeChromosome 21 (human)Edwards SyndromeChromosome 18 (human)Patau SyndromeChromosome 13 (human)Trisomy 9Trisomy 8Chromosome 8 (human)Cat Eye SyndromeTrisomy 22Chromosome 22 (human)Trisomy 16Deletion (genetics)1q21.1 Deletion Syndrome1q21.1 Duplication SyndromeTAR SyndromeChromosome 1 (human)Wolf–Hirschhorn SyndromeChromosome 4 (human)Cri Du ChatChromosome 5q Deletion SyndromeChromosome 5 (human)Williams SyndromeChromosome 7 (human)Jacobsen SyndromeChromosome 11 (human)Miller–Dieker SyndromeSmith–Magenis SyndromeChromosome 17 (human)DiGeorge SyndromeChromosome 22 (human)22q11.2 Distal Deletion SyndromeChromosome 22 (human)22q13 Deletion SyndromeChromosome 22 (human)Genomic ImprintingAngelman SyndromePrader–Willi SyndromeChromosome 15 (human)Distal 18q-Proximal 18q-X ChromosomeY ChromosomeTurner SyndromeTrisomyTetrasomyAneuploidyMosaic (genetics)Klinefelter SyndromeXXYY SyndromeXXXY Syndrome49, XXXXY SyndromeTriple X SyndromeTetrasomy X49, XXXXXXYY Syndrome45,X/46,XY MosaicismChromosomal TranslocationLeukemiaLymphomaBurkitt's LymphomaMycIGH@Follicular LymphomaIGH@Bcl-2Mantle Cell LymphomaMultiple MyelomaCyclin D1IGH@Anaplastic Large-cell LymphomaAnaplastic Lymphoma KinaseNPM1Acute Lymphoblastic LeukemiaPhiladelphia ChromosomeABL (gene)BCR (gene)Acute Myeloblastic Leukemia With MaturationRUNX1T1RUNX1Acute Promyelocytic LeukemiaPromyelocytic Leukemia ProteinRetinoic Acid Receptor AlphaAcute Megakaryoblastic LeukemiaRBM15MKL1Ewing's SarcomaFLI1Ewing Sarcoma Breakpoint Region 1Synovial SarcomaSynaptotagmin 1Synovial Sarcoma, X BreakpointDermatofibrosarcoma ProtuberansCollagen, Type I, Alpha 1PDGFBMyxoid LiposarcomaDNA Damage-inducible Transcript 3FUS (gene)Desmoplastic Small-round-cell TumorWT1Ewing Sarcoma Breakpoint Region 1Alveolar RhabdomyosarcomaPAX3FOXO1PAX7FOXO1Fragile X SyndromeUniparental DisomyXX Male Syndrome46,XX Testicular Disorders Of Sex DevelopmentMarker ChromosomeRing ChromosomeRing Chromosome 14 SyndromeRing Chromosome 18Ring Chromosome 20 SyndromeHelp:CategoryCategory:CytogeneticsCategory:Chromosomal AbnormalitiesCategory:Infobox Medical ConditionDiscussion About Edits From This IP Address [n]A List Of Edits Made From This IP Address [y]View The Content Page [c]Discussion About The Content Page [t]Edit This Page [e]Visit The Main Page [z]Guides To Browsing WikipediaFeatured Content – The Best Of WikipediaFind Background Information On Current EventsLoad A Random Article [x]Guidance On How To Use And Edit WikipediaFind Out About WikipediaAbout The Project, What You Can Do, Where To Find ThingsA List Of Recent Changes In The Wiki [r]List Of All English Wikipedia Pages Containing Links To This Page [j]Recent Changes In Pages Linked From This Page [k]Upload Files [u]A List Of All Special Pages [q]Wikipedia:AboutWikipedia:General Disclaimer

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