Literature DB >> 19800077

Maternal uniparental disomy 14 syndrome demonstrates prader-willi syndrome-like phenotype.

Kana Hosoki1, Masayo Kagami, Touju Tanaka, Masaya Kubota, Kenji Kurosawa, Mitsuhiro Kato, Kimiaki Uetake, Jun Tohyama, Tsutomu Ogata, Shinji Saitoh.   

Abstract

OBJECTIVE: To delineate the significance of maternal uniparental disomy 14 (upd(14)mat) and related disorders in patients with a Prader-Willi syndrome (PWS)-like phenotype. STUDY
DESIGN: We examined 78 patients with PWS-like phenotype who lacked molecular defects for PWS. The MEG3 methylation test followed by microsatellite polymorphism analysis of chromosome 14 was performed to detect upd(14)mat or other related abnormalities affecting the 14q32.2-imprinted region.
RESULTS: We identified 4 patients with upd(14)mat and 1 patient with an epimutation in the 14q32.2 imprinted region. Of the 4 patients with upd(14)mat, 3 had full upd(14)mat and 1 was mosaic.
CONCLUSIONS: Upd(14)mat and epimutation of 14q32.2 represent clinically discernible phenotypes and should be designated "upd(14)mat syndrome." This syndrome demonstrates a PWS-like phenotype particularly during infancy. The MEG3 methylation test can detect upd(14)mat syndrome defects and should therefore be performed for all undiagnosed infants with hypotonia.

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Year:  2009        PMID: 19800077     DOI: 10.1016/j.jpeds.2009.06.045

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


  20 in total

1.  Genomic Analyses of Patients With Unexplained Early-Onset Scoliosis.

Authors:  Xiaochong Gao; Garrett Gotway; Karl Rathjen; Charles Johnston; Steven Sparagana; Carol A Wise
Journal:  Spine Deform       Date:  2014-08-27

2.  Genomic imprinting of DIO3, a candidate gene for the syndrome associated with human uniparental disomy of chromosome 14.

Authors:  Maria Elena Martinez; David F Cox; Brian P Youth; Arturo Hernandez
Journal:  Eur J Hum Genet       Date:  2016-06-22       Impact factor: 4.246

Review 3.  An Update on Molecular Diagnostic Testing of Human Imprinting Disorders.

Authors:  Daria Grafodatskaya; Sanaa Choufani; Raveen Basran; Rosanna Weksberg
Journal:  J Pediatr Genet       Date:  2016-11-10

4.  Placenta-imprinted gene expression association of infant neurobehavior.

Authors:  Carmen J Marsit; Luca Lambertini; Matthew A Maccani; Devin C Koestler; E Andres Houseman; James F Padbury; Barry M Lester; Jia Chen
Journal:  J Pediatr       Date:  2011-12-06       Impact factor: 4.406

5.  Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1.

Authors:  Laïla El Khattabi; Fabien Guimiot; Eva Pipiras; Joris Andrieux; Clarisse Baumann; Sonia Bouquillon; Anne-Lise Delezoide; Bruno Delobel; Florence Demurger; Hélène Dessuant; Séverine Drunat; Christelle Dubourg; Céline Dupont; Laurence Faivre; Muriel Holder-Espinasse; Sylvie Jaillard; Hubert Journel; Stanislas Lyonnet; Valérie Malan; Alice Masurel; Nathalie Marle; Chantal Missirian; Alexandre Moerman; Anne Moncla; Sylvie Odent; Orazio Palumbo; Pietro Palumbo; Aimé Ravel; Serge Romana; Anne-Claude Tabet; Mylène Valduga; Marie Vermelle; Massimo Carella; Jean-Michel Dupont; Alain Verloes; Brigitte Benzacken; Andrée Delahaye
Journal:  Eur J Hum Genet       Date:  2014-11-05       Impact factor: 4.246

6.  A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male.

Authors:  Page L Sorensen; Kirin Basuta; Guadalupe Mendoza-Morales; Louise W Gane; Andrea Schneider; Randi Hagerman; Flora Tassone
Journal:  Am J Med Genet A       Date:  2012-04-09       Impact factor: 2.802

Review 7.  Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.

Authors:  Dai Yang-Li; Luo Fei-Hong; Zhang Hui-Wen; Ma Ming-Sheng; Luo Xiao-Ping; Liu Li; Wang Yi; Zhou Qing; Jiang Yong-Hui; Zou Chao-Chun
Journal:  Orphanet J Rare Dis       Date:  2022-06-13       Impact factor: 4.303

8.  The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome.

Authors:  Yonatan Stelzer; Ido Sagi; Ofra Yanuka; Rachel Eiges; Nissim Benvenisty
Journal:  Nat Genet       Date:  2014-05-11       Impact factor: 38.330

9.  Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami-Ogata syndrome).

Authors:  Masayo Kagami; Kenji Kurosawa; Osamu Miyazaki; Fumitoshi Ishino; Kentaro Matsuoka; Tsutomu Ogata
Journal:  Eur J Hum Genet       Date:  2015-02-18       Impact factor: 4.246

Review 10.  Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci.

Authors:  Thomas Eggermann; Guiomar Perez de Nanclares; Eamonn R Maher; I Karen Temple; Zeynep Tümer; David Monk; Deborah J G Mackay; Karen Grønskov; Andrea Riccio; Agnès Linglart; Irène Netchine
Journal:  Clin Epigenetics       Date:  2015-11-14       Impact factor: 6.551

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