Literature DB >> 14752208

Tall stature, insulin resistance, and disturbed behavior in a girl with the triple X syndrome harboring three SHOX genes: offspring of a father with mosaic Klinefelter syndrome but with two maternal X chromosomes.

Christina Kanaka-Gantenbein1, Sophia Kitsiou, Ariadni Mavrou, Lela Stamoyannou, Aggeliki Kolialexi, Kyriaki Kekou, Magda Liakopoulou, George Chrousos.   

Abstract

AIMS: To describe the tall stature and its possible underlying mechanism in a Caucasian girl (age 12 years and 10 months) with 46,XX (28%)/47,XXX (72%) mosaicism and to identify the parental origin of her extra X chromosome.
METHODS: The fasting glucose-to-insulin ratio was studied. The karyotypes of the girl and her parents as well as the presence of SHOX copies and the parental origin of her extra X chromosome were assessed.
RESULTS: Clinical examination revealed a tall stature and severe acne, and endocrinological/metabolic assessment revealed insulin resistance. Fluorescence in situ hybridization cytogenetic analysis depicted the presence of three SHOX genes in the 47,XXX cell line of the patient. Karyotyping of her parents showed a normal 46,XX karyotype in the mother and 46,XY(93%)/47,XXY(7%) Klinefelter mosaicism in the father. However, DNA analysis unequivocally showed maternal origin of the extra X chromosome of the patient.
CONCLUSIONS: This report suggests that SHOX gene triplication may produce a tall stature, even in the presence of preserved ovarian function. X triplication might predispose to insulin resistance and behavioral disorders. Copyright 2004 S. Karger AG, Basel

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14752208     DOI: 10.1159/000076532

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  7 in total

1.  Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy.

Authors:  Anne Marie Ottesen; Lise Aksglaede; Inger Garn; Nicole Tartaglia; Flora Tassone; Claus H Gravholt; Anders Bojesen; Kaspar Sørensen; Niels Jørgensen; Ewa Rajpert-De Meyts; Tommy Gerdes; Anne-Marie Lind; Susanne Kjaergaard; Anders Juul
Journal:  Am J Med Genet A       Date:  2010-05       Impact factor: 2.802

Review 2.  Triple X syndrome: a review of the literature.

Authors:  Maarten Otter; Constance T R M Schrander-Stumpel; Leopold M G Curfs
Journal:  Eur J Hum Genet       Date:  2009-07-01       Impact factor: 4.246

Review 3.  Height matters-from monogenic disorders to normal variation.

Authors:  Claudia Durand; Gudrun A Rappold
Journal:  Nat Rev Endocrinol       Date:  2013-01-22       Impact factor: 43.330

4.  Acromegaloidism with normal growth hormone secretion associated with X-tetrasomy.

Authors:  Paula Alvarez-Vázquez; Alberto Rivera; Irene Figueroa; Concepción Páramo; Ricardo V García-Mayor
Journal:  Pituitary       Date:  2006       Impact factor: 4.107

Review 5.  Effects of sex chromosome aneuploidies on brain development: evidence from neuroimaging studies.

Authors:  Rhoshel K Lenroot; Nancy Raitano Lee; Jay N Giedd
Journal:  Dev Disabil Res Rev       Date:  2009

6.  Triple X syndrome in a patient with partial lipodystrophy discovered using a high-density oligonucleotide microarray: a case report.

Authors:  Matthew B Lanktree; I George Fantus; Robert A Hegele
Journal:  J Med Case Rep       Date:  2009-08-12

7.  Identification of novel SHOX target genes in the developing limb using a transgenic mouse model.

Authors:  Katja U Beiser; Anne Glaser; Kerstin Kleinschmidt; Isabell Scholl; Ralph Röth; Li Li; Norbert Gretz; Gunhild Mechtersheimer; Marcel Karperien; Antonio Marchini; Wiltrud Richter; Gudrun A Rappold
Journal:  PLoS One       Date:  2014-06-02       Impact factor: 3.240

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.