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[The 49,XYYYY syndrome: apropos of a case detected at birth and followed for 2 1/2 years].

作者信息

Plauchu H, Charrin C, Kossmann J C

出版信息

J Genet Hum. 1984 Sep;32(4):299-306.

PMID:6491641
Abstract

A male child, mentally and physically retarded shows a facial dysmorphy, fingers' abnormalities and a radio-ulnar synostosis. These features are common in the 49,XYYYY syndrom, in which external genitalia, normal at birth, remain undevelopped at the time of puberty. Four others publications through the literature report tetrasomic cells for Y chromosome, but only two of them are real 49,XYYYY (with 88% to 100% of affected cells). Our case has 96,7% tetrasomic cells.

摘要

相似文献

1
[The 49,XYYYY syndrome: apropos of a case detected at birth and followed for 2 1/2 years].
J Genet Hum. 1984 Sep;32(4):299-306.
2
A 49,XXXYY male.一名49,XXXYY男性。
Am J Med Genet. 1981;10(4):351-5. doi: 10.1002/ajmg.1320100407.
3
[Sex chromosome aberration with the 48 XYYY karyotype. A case report of the phenotype of a rare sex chromosome aneuploidy].[48,XYYY核型的性染色体畸变。罕见性染色体非整倍体表型的病例报告]
Z Kinder Jugendpsychiatr. 1994 Jun;22(2):130-4.
4
[Tetra-X syndrome with epilepsy, mental retardation and multiple dysmorphias].[伴有癫痫、智力障碍和多种畸形的四X综合征]
Klin Padiatr. 1993 Mar-Apr;205(2):127-9. doi: 10.1055/s-2007-1025212.
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[Two new cases of partial monosomy 11q with breakpoint in 11q24 (author's transl)].两例11q部分单体性伴11q24断点的新病例(作者译)
Ann Genet. 1979;22(4):239-41.
6
Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism.嵌合型46,XY/47,XY,+der(18)t(Y;18)(q11.22;q11.2)核型、中度智力发育迟缓及非特异性畸形。
Genet Couns. 1990;1(2):173-7.
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Sensorineural deafness in the FG syndrome: report on four new cases.FG综合征中的感音神经性耳聋:4例新病例报告
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8
[Chromosome X-linked mental retardation and marfanoid syndrome].[X染色体连锁智力迟钝与马方综合征样综合征]
J Genet Hum. 1988 Jan;36(1-2):123-8.
9
The 49XXXXX syndrome. Report of a case with 48XXXX/49XXXXX mosaicism.
Acta Paediatr Scand. 1979 Sep;68(5):769-71.
10
A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome.
Clin Dysmorphol. 1993 Jul;2(3):225-31.

引用本文的文献

1
Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature.与49,XYYYY相关的自闭症谱系障碍:病例报告及文献综述
BMC Med Genet. 2017 Jan 31;18(1):9. doi: 10.1186/s12881-017-0371-1.
2
Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes.人类和小鼠性染色体上核糖体蛋白S4基因的结构与功能
Mol Cell Biol. 1994 Apr;14(4):2485-92. doi: 10.1128/mcb.14.4.2485-2492.1994.