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The phenotypic effects of small, distal Xq deletions.

作者信息

Trunca C, Therman E, Rosenwaks Z

出版信息

Hum Genet. 1984;68(1):87-9. doi: 10.1007/BF00293879.

DOI:10.1007/BF00293879
PMID:6500561
Abstract

The effects of small, distal Xq deletions (Xq26----qter) have been reviewed in light of three cases of our own and five from the literature. The symptoms caused by such deletions range from apparently none through irregular menstruation to secondary amenorrhea (or premature menopause) to primary amenorrhea. That the abnormal chromosome has any effects when it is inactivated may best be explained by one or by a combination of the following hypotheses. (1) the Xq-chromosome might exert an effect during development when cells in which it is active compete with cells in which it is inactivated, assuming that the inactivation of the two X chromosomes is originally random. (2) a more probable hypothesis is that there is a position effect when a break has occurred in the critical region Xq13----q27 which apparently must be intact in both X chromosomes to allow normal development of the ovaries. (3) this position effect might, in turn, affect the oocytes (and thus the ovary) after the inactive X chromosome is reactivated before meiosis or the deletion as such might have a direct effect on the ovaries.

摘要

相似文献

1
The phenotypic effects of small, distal Xq deletions.
Hum Genet. 1984;68(1):87-9. doi: 10.1007/BF00293879.
2
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Hum Genet. 1990 Jul;85(2):175-83. doi: 10.1007/BF00193192.
3
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J Med Genet. 1982 Dec;19(6):463-5. doi: 10.1136/jmg.19.6.463.
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Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions.

本文引用的文献

1
X chromosome constitution and the human female phenotype.X染色体构成与人类女性表型。
Hum Genet. 1980;54(2):133-43. doi: 10.1007/BF00278961.
2
Structural anomalies of the X chromosome: personal observation and review of non-mosaic cases.X染色体的结构异常:个人观察及非嵌合病例综述
Clin Genet. 1982 Feb;21(2):145-59. doi: 10.1111/j.1399-0004.1982.tb00752.x.
3
Premature menopause due to a small deletion in the long arm of the X chromosome: a report of three cases and a review.
先证者及其母亲的X染色体缺失(X)(q26.1→q28):分子特征分析及表型-核型推断
Am J Hum Genet. 1993 Mar;52(3):463-71.
4
Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.特纳综合征与女性性染色体畸变:推导临床特征发展中涉及的主要因素。
Hum Genet. 1995 Jun;95(6):607-29. doi: 10.1007/BF00209476.
5
Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.两姐妹在Xq26/Xq27界面处存在远端缺失:DNA研究表明存在IX因子的基因座。
Hum Genet. 1987 May;76(1):54-7. doi: 10.1007/BF00283050.
6
A duplication/deficient X chromosome in a girl with mental retardation and dysmorphic features.一名患有智力障碍和畸形特征的女孩存在一条重复/缺失的X染色体。
J Med Genet. 1988 Apr;25(4):264-7. doi: 10.1136/jmg.25.4.264.
7
The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.人类女性中Xp和Xq缺失所导致的表型效应的相似性:一种假说。
Hum Genet. 1990 Jul;85(2):175-83. doi: 10.1007/BF00193192.
8
Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.一名患有Xq27间质缺失的智力发育迟缓女孩的异常X染色体失活:对脆性X综合征的启示。
Hum Genet. 1990 Mar;84(4):347-52. doi: 10.1007/BF00196232.
9
Short stature in a girl with a terminal Xp deletion distal to DXYS15: localisation of a growth gene(s) in the pseudoautosomal region.一名患有DXYS15远端Xp末端缺失的女孩身材矮小:生长基因在拟常染色体区域的定位
J Med Genet. 1992 Jul;29(7):455-9.
Am J Obstet Gynecol. 1982 Apr 15;142(8):968-72. doi: 10.1016/0002-9378(82)90776-1.
4
Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function.
Hum Genet. 1982;62(3):210-3. doi: 10.1007/BF00333520.
5
Brief clinical report: del(X) (q26) in a phenotypically normal woman and her daughter who also has trisomy 21.
Am J Med Genet. 1983 Feb;14(2):367-72. doi: 10.1002/ajmg.1320140217.
6
X inactivation in man: a woman with t(Xq--;12q+).人类的X染色体失活:一名患有t(Xq--;12q+)的女性。
Am J Hum Genet. 1973 May;25(3):262-70.
7
X-autosome translocations: a review.
Birth Defects Orig Artic Ser. 1978;14(6C):219-47.