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Disease: Monosomy 8q21 q22

  • DNA sequence copy number increase at 8q: a potential new prognostic marker in high-grade osteosarcoma
  • Genomic imbalances during transformation from follicular lymphoma to diffuse large B-cell lymphoma
  • Identification of chromosomal aberrations associated with disease progression and a novel 3q13.31 deletion involving LSAMP gene in osteosarcoma
  • Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant
  • Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant
  • Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses
  • The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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