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Partial trisomy 4q syndrome: case report and review.

作者信息

Cervenka J, Djavadi G R, Gorlin R J

出版信息

Hum Genet. 1976 Sep 10;34(1):1-7. doi: 10.1007/BF00284426.

DOI:10.1007/BF00284426
PMID:964997
Abstract

This communication contributes an additional case of partial trisomy for the long arm of chromosome 4[46,XX,t(X;4)(Q27;Q25)]. Three generations of the patient's family were karyotyped and her mother and brother were found to be balanced translocation carriers. From the patient's clinical examination and from review of 13 similar cases reported in the literature, the following phenotype emerged: constant features were psychomotor retardation, muscle hypotonia at birth, undescended testes in all males and abnormal auricles, typically with a prominent antitragus. Anomalies of kidneys and other structures of the urinary system were present consistently as probably the most characteristic feature of the syndrome. Over 200 structural anomalies of other systems were reported, many of the common to other autosomal chromosomal syndromes.

摘要

相似文献

1
Partial trisomy 4q syndrome: case report and review.
Hum Genet. 1976 Sep 10;34(1):1-7. doi: 10.1007/BF00284426.
2
Partial trisomy 4q due to familial 2/4 translocation.
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3
Partial trisomy 4q: two cases resulting from a familial translocation t(4;18)(q27;p11).4q部分三体综合征:两例源于家族性易位t(4;18)(q27;p11) 。
Hum Genet. 1979 Nov 1;52(1):85-90. doi: 10.1007/BF00284601.
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Trisomy 6q25 leads to 6qter in two sisters resulting from maternal 6;11 translocation.6号染色体长臂25区三体导致两名姐妹出现6号染色体长臂末端异常,这是由母亲的6号与11号染色体易位引起的。
Am J Med Genet. 1980;5(2):171-8. doi: 10.1002/ajmg.1320050211.
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Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes.由于易位染色体的异常分离导致的13号染色体部分三体加4号染色体长臂部分三体。
Clin Genet. 1979 Feb;15(2):176-82. doi: 10.1111/j.1399-0004.1979.tb01758.x.
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A family with a high risk of segregation for an autosomal unbalanced reciprocal translocation.
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引用本文的文献

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A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature.遗传性 t(4;10)(q26;q26.2) 染色体易位病例的多重染色体和分子分析。病例报告及文献复习。
Genes (Basel). 2021 Dec 7;12(12):1957. doi: 10.3390/genes12121957.
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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.
3
Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.

本文引用的文献

1
A FAMILIAL 4/5 RECIPROCAL TRANSLOCATION RESULTING IN PARTIAL TRISOMY B.一个导致部分三体B的家族性4/5相互易位
Am J Hum Genet. 1965 Jan;17(1):54-70.
2
Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.人染色体的喹吖因氮芥荧光:异常易位的特征
Am J Hum Genet. 1972 Mar;24(2):189-213.
3
[Partial B trisomy in cat-cry-syndrome (author's transl)].猫叫综合征中的部分B三体(作者译)
相互易位:一种通过粗线期图绘制预测不平衡分离模式的方法。
Hum Genet. 1980;55(2):209-22. doi: 10.1007/BF00291769.
4
Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.一名患有杜氏肌营养不良症的女性中的(X;6)易位:对DMD基因座定位的影响
J Med Genet. 1981 Dec;18(6):442-7. doi: 10.1136/jmg.18.6.442.
5
X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter.一名可育女性及其47,XXX不育女儿中存在断点位于Xq22的X-常染色体易位。
Hum Genet. 1981;59(4):290-6. doi: 10.1007/BF00295460.
6
X-autosome translocations: cytogenetic characteristics and their consequences.X染色体与常染色体易位:细胞遗传学特征及其后果
Hum Genet. 1982;61(4):295-309. doi: 10.1007/BF00276593.
7
Partial 4q duplication due to inherited der(13),t(4;13)(q26;q34)mat in a girl with a deficiency of factor X.
Hum Genet. 1980;53(3):303-4. doi: 10.1007/BF00287045.
8
Nondisjunction of a translocation-chromosome t(4;13).
Hum Genet. 1981;59(4):337-41. doi: 10.1007/BF00295467.
9
DNA replication and inactivation patterns in structural abnormality of sex chromosomes. I.X-A translocations, rings, fragments, isochromosomes, and pseudo-isodicentrics.性染色体结构异常中的DNA复制与失活模式。I. X-A易位、环状染色体、片段、等臂染色体及假等臂双着丝粒染色体。
Hum Genet. 1984;67(1):37-47. doi: 10.1007/BF00270556.
10
Balanced structural changes involving the human X: effect on sexual phenotype.涉及人类X染色体的平衡结构变化:对性表型的影响
Hum Genet. 1983;63(3):216-21. doi: 10.1007/BF00284652.
Padiatr Padol. 1973;8(4):362-71.
4
Partial trisomy 4 resulting from a 4-18 reciprocal translocation.由4号与18号染色体相互易位导致的4号染色体部分三体。
Ann Genet. 1972 Sep;15(3):191-4.
5
Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus).由于父亲的平衡易位t(4q减;18q加)导致的4q部分三体和18q部分单体。
Humangenetik. 1974;25(3):227-33. doi: 10.1007/BF00281431.
6
Translocation, t(4qminus;13qplus), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation.三代中出现的易位,t(4q减;13q加),导致第四代染色体4长臂部分三体。
J Med Genet. 1974 Jun;11(2):201-5. doi: 10.1136/jmg.11.2.201.
7
Segregating reciprocal (4;21) (q21;q21) translocation with proposita trisomic for parts of 4q and 21.分离出与先证者相关的相互易位(4;21)(q21;q21),先证者部分4q和21三体。
J Med Genet. 1973 Dec;10(4):384-9. doi: 10.1136/jmg.10.4.384.
8
A simple technique for demonstrating centromeric heterochromatin.一种用于显示着丝粒异染色质的简单技术。
Exp Cell Res. 1972 Nov;75(1):304-6. doi: 10.1016/0014-4827(72)90558-7.
9
A rapid banding technique for human chromosomes.一种用于人类染色体的快速显带技术。
Lancet. 1971 Oct 30;2(7731):971-2. doi: 10.1016/s0140-6736(71)90287-x.
10
[Phenotypic variation in partial trisomy 4q (author's transl)].4q部分三体的表型变异(作者译)
Humangenetik. 1975 Jun 19;28(2):103-12. doi: 10.1007/BF00735742.