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. 1974 Mar;11(1):104–108. doi: 10.1136/jmg.11.1.104

Presumptive Mosaic Partial Trisomy Associated with Congenital Anomalies and Mental Deficiency

Angela M Vianna-Morgante , Wanderley M Domingues , Claudio C Ortega , Sanae Kasahara
PMCID: PMC1013097  PMID: 4134623

Abstract

The case of a mentally retarded patient with congenital anomalies not typical of any known chromosome unbalance is reported. In his karyotype, 40·6% of the cells were normal, while 59·4% had a missing G and an almost metacentric marker longer than an F chromosome. The abnormal cell line was interpreted as resulting from a chromatid translocation involving the short arm of a No. 22 and a segment from an unidentified chromosome. The translocation probably took place after the first cell division and was followed by segregation of the translocated chromatids. Other obvious hypotheses were excluded by the study of fluorescence patterns. The patient's clinical features may be due to a partial autosomal trisomy.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Caspersson T., Lomakka G., Zech L. The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability. Hereditas. 1972;67(1):89–102. doi: 10.1111/j.1601-5223.1971.tb02363.x. [DOI] [PubMed] [Google Scholar]
  2. WALKER N. F. The use of dermal configurations in the diagnosis of mongolism. J Pediatr. 1957 Jan;50(1):19–26. doi: 10.1016/s0022-3476(57)80005-5. [DOI] [PubMed] [Google Scholar]

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