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Deletion of the long arm of chromosome 11 [46,XX,del(11)(q24.1--qter)].

作者信息

O'Hare A E, Grace E, Edmunds A T

出版信息

Clin Genet. 1984 Apr;25(4):373-7. doi: 10.1111/j.1399-0004.1984.tb02007.x.

DOI:10.1111/j.1399-0004.1984.tb02007.x
PMID:6713716
Abstract

A child who presented at three months of age with pyloric stenosis and pancytopenia was found to have a partial deletion of the long arm of chromosome 11, del(11)(q24.1----qter). Only two previous cases have been described with an apparently identical chromosomal deletion, and both exhibit similar phenotypic features. Other patients with larger deletions of the distal region of the long arm of chromosome 11 show many features in common with these three cases. It is suggested that the region of the long arm of chromosome 11 from band q24.1 to qter may contain the genetic material responsible for the expression of the 11q - phenotype.

摘要

相似文献

1
Deletion of the long arm of chromosome 11 [46,XX,del(11)(q24.1--qter)].
Clin Genet. 1984 Apr;25(4):373-7. doi: 10.1111/j.1399-0004.1984.tb02007.x.
2
Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
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Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.10号染色体长臂末端缺失:从q26至qter。病例报告及文献复习。
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Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3 --> qter, and trisomy 8q24.3 --> qter.患有联合细胞免疫缺陷、全血细胞减少、畸形、11号染色体长臂23.3区至末端缺失以及8号染色体长臂24.3区至末端三体的女孩。
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Brief clinical report: deletion of the long arm of chromosome 11, [del(11)(q23)].简要临床报告:11号染色体长臂缺失,[del(11)(q23)] 。
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Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].
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引用本文的文献

1
Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.雅各布森综合征:1例伴有严重眼部异常、生长激素缺乏及甲状腺功能减退且与11号染色体(q23q25)缺失相关的患者报告及52例病例回顾
J Med Genet. 1996 Sep;33(9):772-8. doi: 10.1136/jmg.33.9.772.
2
Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation.一例死产儿,伴有含肝脏的脐膨出、短肢及宫内生长迟缓,存在3q部分重复和11q远端缺失。
J Med Genet. 1996 Jul;33(7):615-7. doi: 10.1136/jmg.33.7.615.
3
Clinical and molecular characterization of patients with distal 11q deletions.
11号染色体长臂远端缺失患者的临床与分子特征
Am J Hum Genet. 1995 Mar;56(3):676-83.
4
Report of a deletion 11 (qter----q23.3) and short review of the literature.11号染色体长臂缺失(qter----q23.3)报告及文献综述
Eur J Pediatr. 1985 Sep;144(3):286-8. doi: 10.1007/BF00451964.
5
Trisomy 4q: 46, xy,-11, +der (11), t(4;11) (q27; q25) pat in a child with multiple congenital anomalies.
Indian J Pediatr. 1988 Mar-Apr;55(2):308-11. doi: 10.1007/BF02722206.
6
Congenital ocular and other systemic abnormalities associated with ring-11 chromosome.与11号环状染色体相关的先天性眼部及其他全身异常。
Graefes Arch Clin Exp Ophthalmol. 1986;224(3):317-20. doi: 10.1007/BF02143078.
7
Assignment of the apolipoprotein A-I gene to 11q23 based on RFLP in a case with a partial deletion of chromosome 11, del(11)(q23.3----qter).在一例11号染色体部分缺失del(11)(q23.3----qter)的病例中,基于限制性片段长度多态性将载脂蛋白A-I基因定位于11q23。
Hum Genet. 1990 Jun;85(1):39-40. doi: 10.1007/BF00276323.
8
A terminal deletion of 11q.11号染色体长臂末端缺失
J Med Genet. 1992 Jul;29(7):511-2.