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del(11q24)

MedGen UID:
273701
•Concept ID:
C1515577
•
Cell or Molecular Dysfunction

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVdel(11q24)

Recent clinical studies

Etiology

Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): a patient report and review.
Van Zutven LJ, van Bever Y, Van Nieuwland CC, Huijbregts GC, Van Opstal D, von Bergh AR, Corel LJ, Tibboel D, Wouters CH, Poddighe PJ
Am J Med Genet A 2009 Jul;149A(7):1468-75. doi: 10.1002/ajmg.a.32714. PMID: 19449434
Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.
Gangarossa S, Mattina T, Romano V, Milana G, Mollica F, Schilirò G
Am J Med Genet 1996 Mar 15;62(2):120-3. doi: 10.1002/(SICI)1096-8628(19960315)62:2<120::AID-AJMG4>3.0.CO;2-#. PMID: 8882392

Diagnosis

A PATIENT WITH PARTIAL CHROMOSOME 12q DUPLICATION AND 10q DELETION.
Saat H, Soysal Y, Kurtgoz S, Ergun MA, Percin EF
Genet Couns 2015;26(4):401-7. PMID: 26852510
Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): a patient report and review.
Van Zutven LJ, van Bever Y, Van Nieuwland CC, Huijbregts GC, Van Opstal D, von Bergh AR, Corel LJ, Tibboel D, Wouters CH, Poddighe PJ
Am J Med Genet A 2009 Jul;149A(7):1468-75. doi: 10.1002/ajmg.a.32714. PMID: 19449434

Prognosis

Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): a patient report and review.
Van Zutven LJ, van Bever Y, Van Nieuwland CC, Huijbregts GC, Van Opstal D, von Bergh AR, Corel LJ, Tibboel D, Wouters CH, Poddighe PJ
Am J Med Genet A 2009 Jul;149A(7):1468-75. doi: 10.1002/ajmg.a.32714. PMID: 19449434
Structure, organization, and chromosomal mapping of the human neurogranin gene (NRGN).
Martínez de Arrieta C, Pérez Jurado L, Bernal J, Coloma A
Genomics 1997 Apr 15;41(2):243-9. doi: 10.1006/geno.1997.4622. PMID: 9143500
Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.
Gangarossa S, Mattina T, Romano V, Milana G, Mollica F, Schilirò G
Am J Med Genet 1996 Mar 15;62(2):120-3. doi: 10.1002/(SICI)1096-8628(19960315)62:2<120::AID-AJMG4>3.0.CO;2-#. PMID: 8882392

Clinical prediction guides

Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): a patient report and review.
Van Zutven LJ, van Bever Y, Van Nieuwland CC, Huijbregts GC, Van Opstal D, von Bergh AR, Corel LJ, Tibboel D, Wouters CH, Poddighe PJ
Am J Med Genet A 2009 Jul;149A(7):1468-75. doi: 10.1002/ajmg.a.32714. PMID: 19449434
Structure, organization, and chromosomal mapping of the human neurogranin gene (NRGN).
Martínez de Arrieta C, Pérez Jurado L, Bernal J, Coloma A
Genomics 1997 Apr 15;41(2):243-9. doi: 10.1006/geno.1997.4622. PMID: 9143500
Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.
Gangarossa S, Mattina T, Romano V, Milana G, Mollica F, Schilirò G
Am J Med Genet 1996 Mar 15;62(2):120-3. doi: 10.1002/(SICI)1096-8628(19960315)62:2<120::AID-AJMG4>3.0.CO;2-#. PMID: 8882392

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