Study on the relationship between cytogenetics and phenotypic effect in Turner’s syndrome

Hu Xiaofeng , Zhu Baosheng , Lin Hanhua , Shu Dan , Tao Deding , Wang Mudi

Current Medical Science ›› 1996, Vol. 16 ›› Issue (4) : 245 -248.

PDF
Current Medical Science ›› 1996, Vol. 16 ›› Issue (4) : 245 -248. DOI: 10.1007/BF02888117
Article

Study on the relationship between cytogenetics and phenotypic effect in Turner’s syndrome

Author information +
History +
PDF

Abstract

The cytogenetics and clinical stigmata in 5 cases of Turner’s syndrome were studied. Three of them were non-mosaic i(Xq) and two with partial monosome of a X chromosome short are (Xp21). whose DNA replication patterns of inactive X chromosome were analyzed by RBG technique. Results showed that differences between the replication patterns in cases of X chromosome deletion (Xp21) and normal females existed; that the behavior of abnormal X expressed nonrandom inactivation. It was suggested that the phenotype may be closely related with both X chromosome replication pattern and its inactivation behavior, which might be useful in genetic counselling.

Keywords

DNA replication / X chromosome / phenotypic effect / Turner’s syndrome

Cite this article

Download citation ▾
Hu Xiaofeng, Zhu Baosheng, Lin Hanhua, Shu Dan, Tao Deding, Wang Mudi. Study on the relationship between cytogenetics and phenotypic effect in Turner’s syndrome. Current Medical Science, 1996, 16(4): 245-248 DOI:10.1007/BF02888117

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

CamargM, CervenkaJ. DNA replication and inactivation patterns in structural abnormality of sex chromosomes. Hum Genet, 1984, 67: 37-37

[2]

t(X:X)DNA 1988, 5(1): 15

[3]

CamargoM, CervenkaJ. Patterns of DNA replication of human chromosomes. II. Replication map and replication model. Am J Hum Genet, 1982, 34: 757-757

[4]

ISCN. An international system for human cytogenetic nomenclature. Cytogenet Cell Genet, 1978, 21: 313-313

[5]

WyssD, DelozierC D, DaniellJ. Structural anomalities of the X chromosome: personal obseration and review of non-mosaic cases. Clin Genet, 1982, 21: 145-145

[6]

ThermanE, SusmanB. The similarity of phenotypic effects caused by Xp and Xq deletion in the human female: a hypothesis. Hum Genet, 1990, 85: 175-175

[7]

TemtamyS A, GhaliI, SalamM A. Karyotype/phenotype correlation in females with short stature. Clin Genet, 1992, 41: 147-147

[8]

ThermanE, SartoG E, PalmercG. Position of the human X inaction center on Xq. Hum Genet, 1979, 50: 59-59

[9]

ThermanE, LaxovaRSusman B. The critical region on the human Xq. Hum Genet, 1990, 85: 455-455

[10]

Midro A T, Kulikowski M, Sawicka A. Familial occurrence of isodicentric X chromosome with different breakpoints. Clin Genet, 1988: 34

AI Summary AI Mindmap
PDF

88

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/