Literature DB >> 10356135

Maternal uniparental disomy 14 as a cause of intrauterine growth retardation and early onset of puberty.

S Fokstuen1, C Ginsburg, M Zachmann, A Schinzel.   

Abstract

Uniparental disomy for particular chromosomes is increasingly recognized as a cause of abnormal phenotypes in humans either as a result of imprinted genes or, in the case of isodisomy, homozygosity of mutated recessive alleles. We report on the occurrence of maternal uniparental disomy for chromosome 14 (matUPD 14) in a 25-year-old woman with a normal karyotype, normal intelligence but low birth weight, short stature, small hands, and early onset of puberty. Comparison of her phenotype with those of 15 previously described liveborn patients with matUPD14 gives further evidence for an imprinted gene region on chromosome 14 and highlights the necessity to consider this cause in children with intrauterine growth retardation and early onset of puberty caused by acceleration of skeletal maturation.

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Year:  1999        PMID: 10356135     DOI: 10.1016/s0022-3476(99)70282-9

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  11 in total

1.  Growth parameters in maternal uniparental disomy 7 and 14.

Authors:  Dieter Kotzot
Journal:  Eur J Pediatr       Date:  2007-01-04       Impact factor: 3.183

2.  Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients.

Authors:  T Eggermann; S Mergenthaler; K Eggermann; A Albers; K Linnemann; C Fusch; M B Ranke; H A Wollmann
Journal:  J Med Genet       Date:  2001-02       Impact factor: 6.318

Review 3.  Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements.

Authors:  D Kotzot
Journal:  J Med Genet       Date:  2001-08       Impact factor: 6.318

4.  Inhibition of adipogenesis and development of glucose intolerance by soluble preadipocyte factor-1 (Pref-1).

Authors:  Kichoon Lee; Josep A Villena; Yang Soo Moon; Kee-Hong Kim; Sunjoo Lee; Chulho Kang; Hei Sook Sul
Journal:  J Clin Invest       Date:  2003-02       Impact factor: 14.808

5.  Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14.

Authors:  Melita D Irving; Karin Buiting; Deniz Kanber; Celia Donaghue; Reiner Schulz; Amaka Offiah; Shehla N Mohammed; Rebecca J Oakey
Journal:  Am J Med Genet A       Date:  2010-08       Impact factor: 2.802

6.  At least ten genes define the imprinted Dlk1-Dio3 cluster on mouse chromosome 12qF1.

Authors:  John P Hagan; Brittany L O'Neill; Colin L Stewart; Serguei V Kozlov; Carlo M Croce
Journal:  PLoS One       Date:  2009-02-05       Impact factor: 3.240

7.  Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity.

Authors:  Yang Soo Moon; Cynthia M Smas; Kichoon Lee; Josep A Villena; Kee-Hong Kim; Eun Jun Yun; Hei Sook Sul
Journal:  Mol Cell Biol       Date:  2002-08       Impact factor: 4.272

8.  Relative frequency of underlying genetic causes for the development of UPD(14)pat-like phenotype.

Authors:  Masayo Kagami; Fumiko Kato; Keiko Matsubara; Tomoko Sato; Gen Nishimura; Tsutomu Ogata
Journal:  Eur J Hum Genet       Date:  2012-02-22       Impact factor: 4.246

Review 9.  The mystery of puberty initiation: genetics and epigenetics of idiopathic central precocious puberty (ICPP).

Authors:  Sofia Leka-Emiri; George P Chrousos; Christina Kanaka-Gantenbein
Journal:  J Endocrinol Invest       Date:  2017-03-01       Impact factor: 5.467

10.  Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability.

Authors:  Shujie Zhang; Haisong Qin; Jin Wang; Luping OuYang; Shiyu Luo; Chunyun Fu; Xin Fan; Jiasun Su; Rongyu Chen; Bobo Xie; Xuyun Hu; Shaoke Chen; Yiping Shen
Journal:  Mol Cytogenet       Date:  2016-08-24       Impact factor: 2.009

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