Literature DB >> 574719

Monosomy 21: a possible stepwise evolution of the karyotype.

D Abeliovich, R Carmi, M Karplus, J Bar-Ziv, M M Cohen.   

Abstract

We describe a female infant with manifestations of complete monosomy for chromosome 21 intrauterine growth retardation, failure to thrive, craniofacial anomalies, arthrogryposis-like features, and psychomotor retardation. Chromosome analysis demonstrated mosaicism for three different cell lines in the various tissues examined; 45,XX,-21/46,XX,del(21)(q11)46,XX. The existence of these three lines suggests a possible explanation for the few cases of "complete monosomy 21" which have been reported.

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Year:  1979        PMID: 574719     DOI: 10.1002/ajmg.1320040311

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion.

Authors:  J R Korenberg; D K Kalousek; G Anneren; S M Pulst; J G Hall; C J Epstein; D R Cox
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

2.  Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.

Authors:  M C Phelan; C C Morton; R E Stevenson; R E Tanzi; G D Stewart; P C Watkins; J F Gusella; J A Amos
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

3.  A case of partial monosomy 21q22.2 associated with Rieger's syndrome.

Authors:  F Nielsen; L Trånebjaerg
Journal:  J Med Genet       Date:  1984-06       Impact factor: 6.318

  3 in total

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