Literature DB >> 15732061

Duplication of chromosome 4q: renal pathology of two siblings.

Taketo Otsuka1, Hidehiko Fujinaka, Masaru Imamura, Yasuki Tanaka, Hiroshi Hayakawa, Shuichi Tomizawa.   

Abstract

We report on two sibs with partial 4q trisomy: dup (4)(q35.2-q31.22) and their renal biopsy findings. Both of them show renal hypoplasia, although their chromosomal aberration lacks the minimal duplicated region 4q22-q23 and/or 4q25-q31.3, which had been shown to be associated with urogenital abnormalities and thumb malformations in previous reports. From the renal biopsy findings, the two sibs were diagnosed as oligonephronia. We summarize the 13 having published cases of duplication of chromosome 4q, and examine which segments have a close relationship to renal hypoplasia. We suggest that renal hypoplasia may be female-prone, and may have a close relationship with duplication of 4q33-q34.

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Year:  2005        PMID: 15732061     DOI: 10.1002/ajmg.a.30643

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  12 in total

1.  Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicism.

Authors:  Lucie Tosca; Sophie Brisset; François M Petit; Laure Lecerf; Ghislaine Rousseau; Cécile Bas; Mireille Laroudie; Marie-Laure Maurin; Sylvie Tapia; Olivier Picone; Sophie Prevot; Michel Goossens; Philippe Labrune; Gérard Tachdjian
Journal:  Eur J Hum Genet       Date:  2010-04-28       Impact factor: 4.246

2.  Congenital anomalies of kidney and hand: a review.

Authors:  Gopalakrishnan Natarajan; Dhanapriya Jeyachandran; Bala Subramaniyan; Dineshkumar Thanigachalam; Arul Rajagopalan
Journal:  Clin Kidney J       Date:  2013-02-03

3.  Upregulation of CPE promotes cell proliferation and tumorigenicity in colorectal cancer.

Authors:  Xing-Hua Liang; Ling-Ling Li; Geng-Gang Wu; Yi-Cheng Xie; Guang-Xian Zhang; Wei Chen; Hai-Feng Yang; Qi-Long Liu; Wen-Hong Li; Wen-Guang He; Yan-Nian Huang; Xian-Cheng Zeng
Journal:  BMC Cancer       Date:  2013-09-05       Impact factor: 4.430

4.  The Transcription Factor Hand1 Is Involved In Runx2-Ihh-Regulated Endochondral Ossification.

Authors:  Lindsay E Laurie; Hiroki Kokubo; Masataka Nakamura; Yumiko Saga; Noriko Funato
Journal:  PLoS One       Date:  2016-02-26       Impact factor: 3.240

5.  Hand2 inhibits kidney specification while promoting vein formation within the posterior mesoderm.

Authors:  Elliot A Perens; Zayra V Garavito-Aguilar; Gina P Guio-Vega; Karen T Peña; Yocheved L Schindler; Deborah Yelon
Journal:  Elife       Date:  2016-11-02       Impact factor: 8.140

Review 6.  Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion: A case report and literature review.

Authors:  Fagui Yue; Yuting Jiang; Yang Yu; Xiao Yang; Hongguo Zhang; Ruizhi Liu; Ruixue Wang
Journal:  Medicine (Baltimore)       Date:  2018-11       Impact factor: 1.889

7.  Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation.

Authors:  A M Mohamed; H T El-Bassyouni; A M El-Gerzawy; S A Hammad; N A Helmy; A K Kamel; S I Ismail; M Y Issa; O Eid; M S Zaki
Journal:  Mol Cytogenet       Date:  2018-11-06       Impact factor: 2.009

8.  Response to Growth Hormone Treatment in a Patient with Insulin-Like Growth Factor 1 Receptor Deletion.

Authors:  Ranim Mahmoud; Ajanta Naidu; Hiba Risheg; Virginia Kimonis
Journal:  J Clin Res Pediatr Endocrinol       Date:  2017-07-17

9.  Chromosomal Abnormalities in Syndromic Orofacial Clefts: Report of Three Children.

Authors:  Rathika Damodara Shenoy; Vijaya Shenoy; Vikram Shetty
Journal:  Case Rep Genet       Date:  2018-09-09

10.  The Transcription Factor HAND1 Is Involved in Cortical Bone Mass through the Regulation of Collagen Expression.

Authors:  Noriko Funato; Yuki Taga; Lindsay E Laurie; Chisa Tometsuka; Masashi Kusubata; Kiyoko Ogawa-Goto
Journal:  Int J Mol Sci       Date:  2020-11-16       Impact factor: 5.923

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