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The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome
Kochi, C; Longui, C. A; Lemos-Marini, S. H. V; Guerra-Junior, G; Melo, M. B; Calliari, L. E. P; Monte, O.
  • Kochi, C; Santa Casa de São Paulo. Faculdade de Ciências Médicas. Departamento de Pediatria. Unidade de Endocrinologia Pediátrica. São Paulo. BR
  • Longui, C. A; Santa Casa de São Paulo. Faculdade de Ciências Médicas. Departamento de Pediatria. Unidade de Endocrinologia Pediátrica. São Paulo. BR
  • Lemos-Marini, S. H. V; Faculdade de Ciências Médicas. CIPED - Departamento de Pediatria. Unidade de Endocrinologia Pediátrica. Campinas. BR
  • Guerra-Junior, G; Faculdade de Ciências Médicas. CIPED - Departamento de Pediatria. Unidade de Endocrinologia Pediátrica. Campinas. BR
  • Melo, M. B; Santa Casa de São Paulo. Faculdade de Ciências Médicas. Departamento de Fisiologia. Laboratório de Medicina Molecular. São Paulo. BR
  • Calliari, L. E. P; Santa Casa de São Paulo. Faculdade de Ciências Médicas. Departamento de Pediatria. Unidade de Endocrinologia Pediátrica. São Paulo. BR
  • Monte, O; Santa Casa de São Paulo. Faculdade de Ciências Médicas. Departamento de Pediatria. Unidade de Endocrinologia Pediátrica. São Paulo. BR
Genet. mol. res. (Online) ; 6(1): 1-7, 2007. tab
Article in English | LILACS | ID: lil-440615
ABSTRACT
Thirty-seven 45 X Turner syndrome patients with confirmed peripheral blood lymphocyte karyotype were initially selected to determine the origin of the retained X chromosome and to correlate it with their parents’ stature. Blood samples were available in 25 families. The parental origin of the X chromosome was determined in 24 informativefamilies through the analysis of the exon 1 - CAG repeat variation of the androgen receptor gene. In 70.8% of the cases, the retained X chromosome was maternal in origin and 29.2% was paternal. When we classified the patients according to maternal (Xm) or paternal (Xp) X chromosome, there was a positive correlation between patients’ and maternal heights only in the Xm group. There was no correlation with paternal height in either group, and a significant correlation with target height was only observed in the Xm group. In conclusion, maternal height is the best variable correlating with the height of 45 X Turner syndrome patients who retain the maternal X chromosome, suggesting a strong influence of genes located on the maternal X chromosome on stature.
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Full text: Available Index: LILACS (Americas) Main subject: Parents / Turner Syndrome / Body Height / Chromosomes, Human, X Limits: Female / Humans / Male Language: English Journal: Genet. mol. res. (Online) Journal subject: Molecular Biology / Genetics Year: 2007 Type: Article Affiliation country: Brazil Institution/Affiliation country: Faculdade de Ciências Médicas/BR / Santa Casa de São Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Parents / Turner Syndrome / Body Height / Chromosomes, Human, X Limits: Female / Humans / Male Language: English Journal: Genet. mol. res. (Online) Journal subject: Molecular Biology / Genetics Year: 2007 Type: Article Affiliation country: Brazil Institution/Affiliation country: Faculdade de Ciências Médicas/BR / Santa Casa de São Paulo/BR