Literature DB >> 7789944

Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.

T Ogata1, N Matsuo.   

Abstract

Although clinical features in Turner syndrome have been well defined, underlying genetic factors have not been clarified. To deduce the factors leading to the development of clinical features, we took the following four steps: (1) assessment of clinical features in classic 45,X Turner syndrome; (2) review of clinical features in various female sex chromosome aberrations (karyotype-phenotype correlations); (3) assessment of factors that could lead to Turner features; and (4) correlation of the clinical features with the effects of specific factors. The results indicate that the clinical features in 45,X and in other female sex chromosome aberrations may primarily be determined by: (1) degree of global non-specific developmental defects caused by quantitative alteration of a euchromatic or non-inactivated region; (2) dosage effect of a pseudoautosomal growth gene(s), a Y-specific growth gene(s), and an Xp-Yp homologous lymphogenic gene(s); and (3) degree of chromosome pairing failure in meiocytes that are destined to develop as oocytes in the absence of SRY. 1991; Grumbach and Conte 1992). However, the pertinent factors have not been determined to date. The method to clarify the factors responsible for the development of the Turner phenotype can be broken down into the following steps: (1) assessment of clinical features in classic 45,X Turner syndrome; (2) review of clinical features in various female sex chromosome aberrations (karyotype-phenotype correlations); (3) assessment of factors that could lead to Turner features; and (4) correlation of the clinical features with the effects of specific factors. If the clinical features in 45,X and in other female sex chromosome aberrations are explained by the effects of specific factors, it can be said that such factors contribute to the development of Turner features. In this paper, we take each of the above steps, and propose the principal factors involved in the development of clinical features in Turner syndrome.

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Year:  1995        PMID: 7789944     DOI: 10.1007/bf00209476

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  313 in total

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Journal:  Hereditas       Date:  1975       Impact factor: 3.271

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Journal:  Lancet       Date:  1960-07-16       Impact factor: 79.321

Review 3.  The critical region on the human Xq.

Authors:  E Therman; R Laxova; B Susman
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

4.  The mortality of human XO embryos.

Authors:  B Santesson; J A BOOK; B Kjessler
Journal:  J Reprod Fertil       Date:  1973-07

5.  Additional evidence of gradual loss of germ cells in the pathogenesis of streak ovaries in Turner's syndrome.

Authors:  L Weiss
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

6.  The Turner phenotype and the different types of human x isochromosome.

Authors:  P G Otto; A M Vianna-Morgante; P A Otto; A Wajntal
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Partial long arm deletion of one X chromosome in a patient with secondary amenorrhea.

Authors:  U Ruthner; S Maschik; F Friedrich; G Breitenecker
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

8.  Secondary amenorrhea associated with balanced X-autosome translocation.

Authors:  F Sauer; R M Greenstein; P Reardon; D H Riddick
Journal:  Obstet Gynecol       Date:  1977-01       Impact factor: 7.661

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Authors:  M V Mashkova; D K Verlinskaia
Journal:  Tsitologiia       Date:  1976-07

10.  Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females.

Authors:  J Levilliers; B Quack; J Weissenbach; C Petit
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

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  34 in total

1.  Two male patients with ring Y: definition of an interval in Yq contributing to Turner syndrome.

Authors:  M Tzancheva; R Kaneva; P Kumanov; G Williams; C Tyler-Smith
Journal:  J Med Genet       Date:  1999-07       Impact factor: 6.318

2.  The Y specific growth gene(s): how does it promote stature?

Authors:  T Ogata; N Matsuo
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

3.  A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions.

Authors:  K L Lachlan; S Youings; T Costa; P A Jacobs; N S Thomas
Journal:  Hum Genet       Date:  2005-11-08       Impact factor: 4.132

4.  Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: a clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata.

Authors:  T Hasegawa; T Ogata; Y Hasegawa; M Honda; T Nagai; Y Fukushima; Y Nakahori; N Matsuo
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

Review 5.  Turner syndrome.

Authors:  Shelli R Kesler
Journal:  Child Adolesc Psychiatr Clin N Am       Date:  2007-07

6.  Collectrin gene screening in Turner syndrome patients with kidney malformation.

Authors:  L Pasquali; G d'Annunzio; R Gastaldi; E Di Battista; V Calcaterra; D Larizza; R Lorini; E D'Amato
Journal:  J Genet       Date:  2009-04       Impact factor: 1.166

Review 7.  Three patients with a 45,X/46,X,psu dic(Xp) karyotype.

Authors:  P Dalton; B Coppin; R James; D Skuse; P Jacobs
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318

8.  Ontogenetic changes of craniofacial complex in Turner syndrome patients treated with growth hormone.

Authors:  Jovana Juloski; Branislav Glisic; Ivana Scepan; Jelena Milasin; Katarina Mitrovic; Marko Babic
Journal:  Clin Oral Investig       Date:  2012-09-23       Impact factor: 3.573

9.  Premature ovarian insufficiency in the XO female mouse on the C57BL/6J genetic background.

Authors:  B Vaz; F El Mansouri; X Liu; T Taketo
Journal:  Mol Hum Reprod       Date:  2020-09-01       Impact factor: 4.025

10.  Cardiovascular anomalies in children and young adults with Ullrich-Turner syndrome the Erlangen experience.

Authors:  Thomas M K Völkl; Karin Degenhardt; Andreas Koch; Diemud Simm; Helmuth G Dörr; Helmut Singer
Journal:  Clin Cardiol       Date:  2005-02       Impact factor: 2.882

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