Literature DB >> 2106786

A ring X chromosome, 46,Y,r(X)(p22.33q28), as a cause of extreme short stature in a male.

T Ogata1, N Matsuo, N Shimizu.   

Abstract

We describe a 15 10/12-year-old boy (Tanner stage 4, peak growth velocity 7 cm/year) with a ring X chromosome who presented with extreme short stature (mean -5.3 SD) as the sole recognizable abnormality. His chromosome constitution was determined to be 46,Y,r(X)(p22.33q28) in 174 of 182 peripheral blood cells and in 35 skin fibroblasts. Of the remaining eight peripheral blood cells, five had a dicentric double-size ring and three had a smaller ring. Other laboratory studies for short stature were noncontributory. We suspect that the ring's specific behavior in mitosis or its effect on expression of the statural determinant on the X chromosome short arm may be responsible for short stature in this patient.

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Year:  1990        PMID: 2106786     DOI: 10.1002/ajmg.1320350219

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


  2 in total

Review 1.  Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

2.  A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation.

Authors:  M Fukami; S Kirsch; S Schiller; A Richter; V Benes; B Franco; K Muroya; E Rao; S Merker; B Niesler; A Ballabio; W Ansorge; T Ogata; G A Rappold
Journal:  Am J Hum Genet       Date:  2000-07-20       Impact factor: 11.025

  2 in total

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