Utente:Adert/SandBox4: differenze tra le versioni

Versione delle 01:16, 10 apr 2016

Versione delle 13:59, 10 apr 2016

Riga 368:

{{Navbox

| name = Chromosomal abnormalities

| title = [[ChromosomeCromosoma abnormality|ChromosomeCromosoma 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

Riga 376:

| group1 = [[Trisomy|Trisomies]]

| list1 = [[Sindrome di Down]] ([[Cromosoma 21|21]]) {{·}} [[Sindrome di Edwards]] ([[Cromosoma 18|18]]) {{·}} [[Sindrome di Patau]] ([[Cromosoma 13|13]]) {{·}} [[Trisomia 9]] {{·}} [[Sindrome di Warkany 2]] ([[Cromosoma 8|8]]) {{·}} [[Sindrome degli occhi di gatto]]/[[Trisomia 22]] ([[Cromosoma 22|22]]) {{·}} [[Trisomia 16]]

| 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]] ([[Cromosoma 1|1]]) {{·}} [[Sindrome di Wolf-Hirschhorn]] ([[Cromosoma 4|4]]) {{·}} [[Cri du chat]]/[[Cromosoma 5q deletion syndrome]] ([[Cromosoma 5|5]]) {{·}} [[Sindrome di Williams-Beuren]] ([[Cromosoma 7|7]]) {{·}} [[Sindrome di Jacobsen]]([[Cromosoma 11|11]]) {{·}} [[Sindrome di Miller-Dieker]]/[[Sindrome di Smith-Magenis]] ([[Cromosoma 17|17]]) {{·}} [[Sindrome da delezione 22q11|Sindrome di DiGeorge]] ([[Cromosoma 22|22]]) {{·}}[[22q11.2 distal deletion syndrome]] ([[Cromosoma 22|22]]) {{·}} [[22q13 deletion syndrome]] ([[Cromosoma 22|22]]) {{·}} ''[[imprinting genomico]]'' ([[Sindrome di Angelman]]/[[Sindrome di Prader-Willi]] ([[Cromosoma 15|15]]) {{·}} [[Distal 18q-]]/[[Proximal 18q-]]

| 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 = [[XCromosoma chromosomeX|X]]/[[YCromosoma chromosomeY|Y]] linked

| list2 = {{Navbox|child

| group1 = [[MonosomyMonosomia]]

| list1 =

*{{·}} [[TurnerSindrome di syndrome|Turner|Sindrome syndromedi Turner (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]]

| group2 = [[TrisomyTrisomia]]/[[tetrasomyTetrasomia]],<br />[[Aneuploidy|other karyotypes]]/[[Mosaic (genetics)|mosaics]]

| list2 = [[Sindrome di Klinefelter|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)]] {{·}} [[Sindrome della quadrupla X|48,XXXX]] {{·}} [[49, XXXXX|49,XXXXX]] {{·}} [[Sindrome 47,XYY|47,XYY]] {{·}} [[48, XYYY|48,XYYY]] {{·}} [[49, XYYYY|49,XYYYY]] {{·}} [[45,X/46,XY mosaicism|45,X/46,XY]]

}}

| group3 = [[ChromosomalTranslocazione translocationcromosomica|TranslocationsTranslocazione]]

| list3 = {{Navbox|child

| group1 = [[LeukemiaLeucemia]]/[[lymphomalinfoma]]

| list1 = {{Navbox|child

| group1 = Lymphoid

| list1 =[[Linfoma di Burkitt]] t(8 [[Myc|MYC]];14 [[IGH@|IGH]]) {{·}} [[Linfoma follicolare]] t(14 [[IGH@|IGH]];18 [[Bcl-2|BCL2]]) {{·}} [[Linfoma mantellare]]/[[Mieloma multiplo]] t(11 [[Cyclin D1|CCND1]]:14 [[IGH@|IGH]]) {{·}} [[Linfoma a grandi cellule anaplastico]] t(2 [[Anaplastic lymphoma kinase|ALK]];5 [[NPM1]]) {{·}} [[Leucemia linfoblastica acuta]]

| 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 = MyeloidMieloide

| list2 =[[Philadelphia Cromosoma]] t(9 [[ABL (gene)|ABL]]; 22 [[BCR (gene)|BCR]]) {{·}} [[Acute myeloblastic leukemia with maturation]] t(8 [[RUNX1T1]];21 [[RUNX1]]) {{·}} [[Leucemia promielocitica acuta]] t(15 [[Promyelocytic leukemia protein|PML]],17 [[Retinoic acid receptor alpha|RARA]]) {{·}} [[Acute megakaryoblastic leukemia]] t(1 [[RBM15]];22 [[MKL1]])

}}

| group2 = OtherAltro

| list2 = [[Sarcoma di Ewing]] t(11 [[FLI1]]; 22 [[Ewing sarcoma breakpoint region 1|EWS]]) {{·}} [[Sarcoma sinoviale]] t(x [[Synaptotagmin 1|SYT]];18 [[Synovial sarcoma, X breakpoint|SSX]]){{·}} [[Dermatofibrosarcoma]] 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]])

| 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 = OtherAltro

| list4 =[[Sindrome dell'X fragile]] {{·}} [[Uniparental disomy]] {{·}} [[XX male syndrome]] {{·}} [[Ring Cromosoma]] (13; [[Ring Cromosoma 14 syndrome|14]]; 15; [[Ring Cromosoma 20 syndrome|20]])

| 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>