Utente:Adert/SandBox4: differenze tra le versioni
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==cc==
{{Navbox
| name = Chromosomal abnormalities
| title = [[Chromosome abnormality|Chromosome abnormalities]] ([[ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities#Q90–Q99 – Chromosomal abnormalities, not elsewhere classified|Q90–Q99]], [[List of ICD-9 codes 740–759: congenital anomalies#Chromosomal anomalies|758]])
| state = {{{state<includeonly>|autocollapse</includeonly>}}}
| listclass = hlist
| group1 = [[Autosome|Autosomal]]
| list1 = {{Navbox|child
| group1 = [[Trisomy|Trisomies]]
| list1 =
* [[Sindrome di Downe]]
** [[Chromosome 21 (human)|21]]
* [[Sindrome di Edwards]]
** [[Chromosome 18 (human)|18]]
* [[Sindrome di Patau]]
** [[Chromosome 13 (human)|13]]
* [[Trisomy 9]]
* [[Trisomy 8|Warkany syndrome 2]]
** [[Chromosome 8 (human)|8]]
* [[Cat eye syndrome]]/[[Trisomy 22]]
** [[Chromosome 22 (human)|22]]
* [[Trisomy 16]]
| group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]]
| list2 =
* [[1q21.1 deletion syndrome]]/[[1q21.1 duplication syndrome]]/[[TAR syndrome]]
** [[Chromosome 1 (human)|1]]
* [[Wolf–Hirschhorn syndrome]]
** [[Chromosome 4 (human)|4]]
* [[Cri du chat]]/[[Chromosome 5q deletion syndrome]]
** [[Chromosome 5 (human)|5]]
* [[Williams syndrome]]
** [[Chromosome 7 (human)|7]]
* [[Jacobsen syndrome]]
** [[Chromosome 11 (human)|11]]
* [[Miller–Dieker syndrome]]/[[Smith–Magenis syndrome]]
** [[Chromosome 17 (human)|17]]
* [[DiGeorge syndrome]]
** [[Chromosome 22 (human)|22]]
* [[22q11.2 distal deletion syndrome]]
** [[Chromosome 22 (human)|22]]
* [[22q13 deletion syndrome]]
** [[Chromosome 22 (human)|22]]
* ''[[genomic imprinting]]''
** [[Angelman syndrome]]/[[Prader–Willi syndrome]] ([[Chromosome 15 (human)|15]])
* [[Distal 18q-]]/[[Proximal 18q-]]
}}
| group2 = [[X chromosome|X]]/[[Y chromosome|Y]] linked
| list2 = {{Navbox|child
| group1 = [[Monosomy]]
| list1 =
* [[Turner syndrome|Turner syndrome (45,X)]]
| group2 = [[Trisomy]]/[[tetrasomy]],<br />[[Aneuploidy|other karyotypes]]/[[Mosaic (genetics)|mosaics]]
| list2 =
* [[Sindrome di Klinefelter syndrome|Sindrome di Klinefelter (47,XXY)]]
* [[XXYY syndrome|48,XXYY]]
* [[XXXY syndrome|48,XXXY]]
* [[49, XXXYY|49,XXXYY]]
* [[49, XXXXY syndrome|49,XXXXY]]
* [[Sindrome della tripla X|Sindrome della tripla X (47,XXX)]]
* [[48, XXXX|48,XXXX]]
* [[49, XXXXX|49,XXXXX]]
* [[XYY syndrome|47,XYY]]
* [[48, XYYY|48,XYYY]]
* [[49, XYYYY|49,XYYYY]]
* [[45,X/46,XY mosaicism|45,X/46,XY]]
}}
| group3 = [[Chromosomal translocation|Translocations]]
| list3 = {{Navbox|child
| group1 = [[Leukemia]]/[[lymphoma]]
| list1 = {{Navbox|child
| group1 = Lymphoid
| list1 =
* [[Burkitt's lymphoma]] t(8 [[Myc|MYC]];14 [[IGH@|IGH]])
* [[Follicular lymphoma]] t(14 [[IGH@|IGH]];18 [[Bcl-2|BCL2]])
* [[Mantle cell lymphoma]]/[[Multiple myeloma]] t(11 [[Cyclin D1|CCND1]]:14 [[IGH@|IGH]])
* [[Anaplastic large-cell lymphoma ]] t(2 [[Anaplastic lymphoma kinase|ALK]];5 [[NPM1]])
* [[Acute lymphoblastic leukemia]]
| group2 = Myeloid
| list2 =
* [[Philadelphia chromosome]] t(9 [[ABL (gene)|ABL]]; 22 [[BCR (gene)|BCR]])
* [[Acute myeloblastic leukemia with maturation]] t(8 [[RUNX1T1]];21 [[RUNX1]])
* [[Acute promyelocytic leukemia]] t(15 [[Promyelocytic leukemia protein|PML]],17 [[Retinoic acid receptor alpha|RARA]])
* [[Acute megakaryoblastic leukemia]] t(1 [[RBM15]];22 [[MKL1]])
}}
| group2 = Other
| list2 =
* [[Ewing's sarcoma]] t(11 [[FLI1]]; 22 [[Ewing sarcoma breakpoint region 1|EWS]])
* [[Synovial sarcoma]] t(x [[Synaptotagmin 1|SYT]];18 [[Synovial sarcoma, X breakpoint|SSX]])
* [[Dermatofibrosarcoma protuberans]] t(17 [[Collagen, type I, alpha 1|COL1A1]];22 [[PDGFB]])
* [[Myxoid liposarcoma]] t(12 [[DNA damage-inducible transcript 3|DDIT3]]; 16 [[FUS]])
* [[Desmoplastic small-round-cell tumor]] t(11 [[WT1]]; 22 [[Ewing sarcoma breakpoint region 1|EWS]])
* [[Alveolar rhabdomyosarcoma]] t(2 [[PAX3]]; 13 [[FOXO1]]) t (1 [[PAX7]]; 13 [[FOXO1]])
}}
| group4 = Other
| list4 =
* [[Fragile X syndrome]]
* [[Uniparental disomy]]
* [[XX male syndrome]]
* [[Ring chromosome]] (13; [[Ring chromosome 14 syndrome|14]]; 15; [[Ring chromosome 20 syndrome|20]])
}}<noinclude>
</noinclude>
| |||