Literature DB >> 30179896

UBE2A-related X-linked intellectual disability.

Roger E Stevenson1, Albert E Chudley2, Anand K Srivastava1, Jayson Rodriguez1, Michael J Friez1, Charles E Schwartz1.   

Abstract

UBE2A-related X-linked intellectual disability is characterized by a distinctive facial phenotype (dense eyebrows and eyelashes, synophrys, hypertelorism, upslanted palpebral fissures, wide mouth, and thin lips), generalized hirsutism, hypoplastic genitalia, short stature, hypotonia, seizures, and severe intellectual disability. Five affected males in two families are described here and compared with the previously reported 17 males in eight families. The new cases are notable for the absence of nail dystrophy, previously considered a defining manifestation, and for the presence of hypogammaglobulinemia and adult-onset ataxia.

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Year:  2019        PMID: 30179896      PMCID: PMC6279472          DOI: 10.1097/MCD.0000000000000242

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  13 in total

1.  Next-generation sequencing in X-linked intellectual disability.

Authors:  Andreas Tzschach; Ute Grasshoff; Stefanie Beck-Woedl; Claudia Dufke; Claudia Bauer; Martin Kehrer; Christina Evers; Ute Moog; Barbara Oehl-Jaschkowitz; Nataliya Di Donato; Robert Maiwald; Christine Jung; Alma Kuechler; Solveig Schulz; Peter Meinecke; Stephanie Spranger; Jürgen Kohlhase; Jörg Seidel; Silke Reif; Manuela Rieger; Angelika Riess; Marc Sturm; Julia Bickmann; Christopher Schroeder; Andreas Dufke; Olaf Riess; Peter Bauer
Journal:  Eur J Hum Genet       Date:  2015-02-04       Impact factor: 4.246

2.  UBE2A deficiency in two siblings: A novel splicing variant inherited from a maternal germline mosaicism.

Authors:  Teresa Giugliano; Claudia Santoro; Annalaura Torella; Francesca Del Vecchio Blanco; Pia Bernardo; Vincenzo Nigro; Giulio Piluso
Journal:  Am J Med Genet A       Date:  2017-12-28       Impact factor: 2.802

3.  Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation.

Authors:  Shozo Honda; Koji O Orii; Junya Kobayashi; Shin Hayashi; Atsushi Imamura; Issei Imoto; Eiji Nakagawa; Yu-ichi Goto; Johji Inazawa
Journal:  J Hum Genet       Date:  2010-03-26       Impact factor: 3.172

4.  UBE2A, which encodes a ubiquitin-conjugating enzyme, is mutated in a novel X-linked mental retardation syndrome.

Authors:  Rafaella M P Nascimento; Paulo A Otto; Arjan P M de Brouwer; Angela M Vianna-Morgante
Journal:  Am J Hum Genet       Date:  2006-07-03       Impact factor: 11.025

5.  UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients.

Authors:  Nicole de Leeuw; Saskia Bulk; Andrew Green; Lane Jaeckle-Santos; Linda A Baker; Andrew R Zinn; Tjitske Kleefstra; Jasper J van der Smagt; Angela Maria Vianne Morgante; Bert B A de Vries; Hans van Bokhoven; Arjan P M de Brouwer
Journal:  Am J Med Genet A       Date:  2010-12       Impact factor: 2.802

6.  Novel missense mutations in the ubiquitination-related gene UBE2A cause a recognizable X-linked mental retardation syndrome.

Authors:  B Budny; M Badura-Stronka; A Materna-Kiryluk; A Tzschach; M Raynaud; A Latos-Bielenska; H H Ropers
Journal:  Clin Genet       Date:  2010-04-19       Impact factor: 4.438

7.  UBE2A deficiency syndrome: a report of two unrelated cases with large Xq24 deletions encompassing UBE2A gene.

Authors:  Sofia Thunstrom; Liv Sodermark; Liz Ivarsson; Lena Samuelsson; Margarita Stefanova
Journal:  Am J Med Genet A       Date:  2014-10-06       Impact factor: 2.802

8.  X-linked intellectual disability type Nascimento is a clinically distinct, probably underdiagnosed entity.

Authors:  Johanna Christina Czeschik; Peter Bauer; Karin Buiting; Claudia Dufke; Encarna Guillén-Navarro; Diana S Johnson; Udo Koehler; Vanesa López-González; Hermann-Josef Lüdecke; Alison Male; Deborah Morrogh; Angelika Rieß; Andreas Tzschach; Dagmar Wieczorek; Alma Kuechler
Journal:  Orphanet J Rare Dis       Date:  2013-09-21       Impact factor: 4.123

9.  A novel UBE2A mutation causes X-linked intellectual disability type Nascimento.

Authors:  Yoshinori Tsurusaki; Ikuko Ohashi; Yumi Enomoto; Takuya Naruto; Jun Mitsui; Noriko Aida; Kenji Kurosawa
Journal:  Hum Genome Var       Date:  2017-06-08

10.  A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.

Authors:  Patrick S Tarpey; Raffaella Smith; Erin Pleasance; Annabel Whibley; Sarah Edkins; Claire Hardy; Sarah O'Meara; Calli Latimer; Ed Dicks; Andrew Menzies; Phil Stephens; Matt Blow; Chris Greenman; Yali Xue; Chris Tyler-Smith; Deborah Thompson; Kristian Gray; Jenny Andrews; Syd Barthorpe; Gemma Buck; Jennifer Cole; Rebecca Dunmore; David Jones; Mark Maddison; Tatiana Mironenko; Rachel Turner; Kelly Turrell; Jennifer Varian; Sofie West; Sara Widaa; Paul Wray; Jon Teague; Adam Butler; Andrew Jenkinson; Mingming Jia; David Richardson; Rebecca Shepherd; Richard Wooster; M Isabel Tejada; Francisco Martinez; Gemma Carvill; Rene Goliath; Arjan P M de Brouwer; Hans van Bokhoven; Hilde Van Esch; Jamel Chelly; Martine Raynaud; Hans-Hilger Ropers; Fatima E Abidi; Anand K Srivastava; James Cox; Ying Luo; Uma Mallya; Jenny Moon; Josef Parnau; Shehla Mohammed; John L Tolmie; Cheryl Shoubridge; Mark Corbett; Alison Gardner; Eric Haan; Sinitdhorn Rujirabanjerd; Marie Shaw; Lucianne Vandeleur; Tod Fullston; Douglas F Easton; Jackie Boyle; Michael Partington; Anna Hackett; Michael Field; Cindy Skinner; Roger E Stevenson; Martin Bobrow; Gillian Turner; Charles E Schwartz; Jozef Gecz; F Lucy Raymond; P Andrew Futreal; Michael R Stratton
Journal:  Nat Genet       Date:  2009-04-19       Impact factor: 38.330

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