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De novo direct duplication 3 (p25-->pter): a previously undescribed chromosomal aberration.

作者信息

Kotzot D, Krüger C, Braun-Quentin C

机构信息

Institute of Human Genetics, University of Erlangen-Nürnberg, Germany.

出版信息

Clin Genet. 1996 Aug;50(2):96-8. doi: 10.1111/j.1399-0004.1996.tb02356.x.

DOI:10.1111/j.1399-0004.1996.tb02356.x
PMID:8937769
Abstract

We report on a case of de novo direct duplication for the distal part of chromosome 3p: 46,XY,dir dup (3) (p25-->pter). At the age of 4 years and 7 months, the boy presented with moderate growth and mental retardation, muscular hypotonia, hypoplasia of the left kidney, a short neck, and a square-shaped face characterized by a broad and flat nasal bridge, slight epicanthus, and full cheeks. So far, only a few cases with such a small distal 3p duplication have been described, and none of them has a de novo direct duplication for this region. In our patient, dysmorphic signs are less impressive, and developmental delay is relatively moderate.

摘要

相似文献

1
De novo direct duplication 3 (p25-->pter): a previously undescribed chromosomal aberration.
Clin Genet. 1996 Aug;50(2):96-8. doi: 10.1111/j.1399-0004.1996.tb02356.x.
2
Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.由于倒位重复和直接重复导致的18号染色体短臂部分三体性
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Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.2号染色体短臂部分重复(dup(2)(p13----p21))与智力发育迟缓及类阿斯克格综合征表型相关。
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Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome.16q11.1至16q13的直接重复与典型的畸形综合征无关。
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46, XY, del (3) (pter-->p25) syndrome: further delineation of the clinical phenotype.46,XY,del(3)(pter→p25)综合征:临床表型的进一步描述。
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[Phenotypic and genetic analysis of a boy with 3p26.3-pter deletion and 7q31.33-qter duplication].[一名患有3p26.3-pter缺失和7q31.33-qter重复的男孩的表型和基因分析]
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