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A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy - case report and review of the literature.

Pavel TesnerJana DrabovaMiroslav StolfaMartin KudrMartin KynclVeronika MoslerovaDrahuse NovotnaRadka Kremlikova PourovaEduard KocarekTereza RasplickovaZdenek SedlacekMarketa Vlckova
Published in: Molecular cytogenetics (2018)
Our observations indicate that for the assessment of prognosis, especially with respect to intellectual functioning, the level of mosaicism could be more important than the extent of amplification and the number of extra copies. Evaluation of the phenotypical effect of rare chromosomal aberrations is challenging and each additional case is valuable for refinement of the genotype-phenotype correlation. Moreover, our patient demonstrates that if the phenotype is severe and if the level of sSMC mosaicism is low in lymphocytes, other tissues should be tested.
Keyphrases
  • copy number
  • case report
  • gene expression
  • minimally invasive
  • early onset
  • dna methylation
  • drug induced
  • clinical evaluation