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del(17q25)

MedGen UID:
273704
•Concept ID:
C1515589
•
Cell or Molecular Dysfunction

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVdel(17q25)

Professional guidelines

PubMed

11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: report from an international workshop.
Bloomfield CD, Archer KJ, Mrózek K, Lillington DM, Kaneko Y, Head DR, Dal Cin P, Raimondi SC
Genes Chromosomes Cancer 2002 Apr;33(4):362-78. doi: 10.1002/gcc.10046. PMID: 11921271

Recent clinical studies

Etiology

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
Armstrong NJ, Mather KA, Sargurupremraj M, Knol MJ, Malik R, Satizabal CL, Yanek LR, Wen W, Gudnason VG, Dueker ND, Elliott LT, Hofer E, Bis J, Jahanshad N, Li S, Logue MA, Luciano M, Scholz M, Smith AV, Trompet S, Vojinovic D, Xia R, Alfaro-Almagro F, Ames D, Amin N, Amouyel P, Beiser AS, Brodaty H, Deary IJ, Fennema-Notestine C, Gampawar PG, Gottesman R, Griffanti L, Jack CR Jr, Jenkinson M, Jiang J, Kral BG, Kwok JB, Lampe L, C M Liewald D, Maillard P, Marchini J, Bastin ME, Mazoyer B, Pirpamer L, Rafael Romero J, Roshchupkin GV, Schofield PR, Schroeter ML, Stott DJ, Thalamuthu A, Trollor J, Tzourio C, van der Grond J, Vernooij MW, Witte VA, Wright MJ, Yang Q, Morris Z, Siggurdsson S, Psaty B, Villringer A, Schmidt H, Haberg AK, van Duijn CM, Jukema JW, Dichgans M, Sacco RL, Wright CB, Kremen WS, Becker LC, Thompson PM, Mosley TH, Wardlaw JM, Ikram MA, Adams HHH, Seshadri S, Sachdev PS, Smith SM, Launer L, Longstreth W, DeCarli C, Schmidt R, Fornage M, Debette S, Nyquist PA
Stroke 2020 Jul;51(7):2111-2121. Epub 2020 Jun 10 doi: 10.1161/STROKEAHA.119.027544. PMID: 32517579Free PMC Article
11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: report from an international workshop.
Bloomfield CD, Archer KJ, Mrózek K, Lillington DM, Kaneko Y, Head DR, Dal Cin P, Raimondi SC
Genes Chromosomes Cancer 2002 Apr;33(4):362-78. doi: 10.1002/gcc.10046. PMID: 11921271
Chromosomal alterations associated with evolution from myelodysplastic syndrome to acute myeloid leukemia.
de Souza Fernandez T, Ornellas MH, Otero de Carvalho L, Tabak D, Abdelhay E
Leuk Res 2000 Oct;24(10):839-48. doi: 10.1016/s0145-2126(00)00056-4. PMID: 10996202

Diagnosis

Acute myeloid leukemia in Baraitser-Winter cerebrofrontofacial syndrome.
Cianci P, Fazio G, Casagranda S, Spinelli M, Rizzari C, Cazzaniga G, Selicorni A
Am J Med Genet A 2017 Feb;173(2):546-549. Epub 2016 Nov 21 doi: 10.1002/ajmg.a.38057. PMID: 27868373
11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: report from an international workshop.
Bloomfield CD, Archer KJ, Mrózek K, Lillington DM, Kaneko Y, Head DR, Dal Cin P, Raimondi SC
Genes Chromosomes Cancer 2002 Apr;33(4):362-78. doi: 10.1002/gcc.10046. PMID: 11921271
Chromosomal alterations associated with evolution from myelodysplastic syndrome to acute myeloid leukemia.
de Souza Fernandez T, Ornellas MH, Otero de Carvalho L, Tabak D, Abdelhay E
Leuk Res 2000 Oct;24(10):839-48. doi: 10.1016/s0145-2126(00)00056-4. PMID: 10996202

Therapy

Acute myeloid leukemia in Baraitser-Winter cerebrofrontofacial syndrome.
Cianci P, Fazio G, Casagranda S, Spinelli M, Rizzari C, Cazzaniga G, Selicorni A
Am J Med Genet A 2017 Feb;173(2):546-549. Epub 2016 Nov 21 doi: 10.1002/ajmg.a.38057. PMID: 27868373

Prognosis

Chromosomal alterations associated with evolution from myelodysplastic syndrome to acute myeloid leukemia.
de Souza Fernandez T, Ornellas MH, Otero de Carvalho L, Tabak D, Abdelhay E
Leuk Res 2000 Oct;24(10):839-48. doi: 10.1016/s0145-2126(00)00056-4. PMID: 10996202

Clinical prediction guides

Diverse mutations and structural variations contribute to Notch signaling deregulation in paediatric T-cell lymphoblastic lymphoma.
Salmerón-Villalobos J, Ramis-Zaldivar JE, Balagué O, Verdú-Amorós J, Celis V, Sábado C, Garrido M, Mato S, Uriz J, Ortega MJ, Gutierrez-Camino A, Sinnett D, Illarregi U, Carron M, Regueiro A, Galera A, Gonzalez-Farré B, Campo E, Garcia N, Colomer D, Astigarraga I, Andrés M, Llavador M, Martin-Guerrero I, Salaverria I
Pediatr Blood Cancer 2022 Nov;69(11):e29926. Epub 2022 Aug 24 doi: 10.1002/pbc.29926. PMID: 36000950
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
Armstrong NJ, Mather KA, Sargurupremraj M, Knol MJ, Malik R, Satizabal CL, Yanek LR, Wen W, Gudnason VG, Dueker ND, Elliott LT, Hofer E, Bis J, Jahanshad N, Li S, Logue MA, Luciano M, Scholz M, Smith AV, Trompet S, Vojinovic D, Xia R, Alfaro-Almagro F, Ames D, Amin N, Amouyel P, Beiser AS, Brodaty H, Deary IJ, Fennema-Notestine C, Gampawar PG, Gottesman R, Griffanti L, Jack CR Jr, Jenkinson M, Jiang J, Kral BG, Kwok JB, Lampe L, C M Liewald D, Maillard P, Marchini J, Bastin ME, Mazoyer B, Pirpamer L, Rafael Romero J, Roshchupkin GV, Schofield PR, Schroeter ML, Stott DJ, Thalamuthu A, Trollor J, Tzourio C, van der Grond J, Vernooij MW, Witte VA, Wright MJ, Yang Q, Morris Z, Siggurdsson S, Psaty B, Villringer A, Schmidt H, Haberg AK, van Duijn CM, Jukema JW, Dichgans M, Sacco RL, Wright CB, Kremen WS, Becker LC, Thompson PM, Mosley TH, Wardlaw JM, Ikram MA, Adams HHH, Seshadri S, Sachdev PS, Smith SM, Launer L, Longstreth W, DeCarli C, Schmidt R, Fornage M, Debette S, Nyquist PA
Stroke 2020 Jul;51(7):2111-2121. Epub 2020 Jun 10 doi: 10.1161/STROKEAHA.119.027544. PMID: 32517579Free PMC Article
Chromosomal alterations associated with evolution from myelodysplastic syndrome to acute myeloid leukemia.
de Souza Fernandez T, Ornellas MH, Otero de Carvalho L, Tabak D, Abdelhay E
Leuk Res 2000 Oct;24(10):839-48. doi: 10.1016/s0145-2126(00)00056-4. PMID: 10996202
Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas.
Nilbert M, Mandahl N, Heim S, Rydholm A, Helm G, Willén H, Baldetorp B, Mitelman F
Cancer Genet Cytogenet 1990 Sep;48(2):217-23. doi: 10.1016/0165-4608(90)90123-r. PMID: 2397453
Cytogenetic analysis of in vitro karyotype evolution in a cell line established from nonmalignant human mammary epithelium.
Nielsen KV, Briand P
Cancer Genet Cytogenet 1989 May;39(1):103-18. doi: 10.1016/0165-4608(89)90236-7. PMID: 2731137

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