Literature DB >> 24166814

Malformations among the X-linked intellectual disability syndromes.

Roger E Stevenson1, Charles E Schwartz, R Curtis Rogers.   

Abstract

Malformations are significant contributions to childhood mortality and disability. Their co-occurrence with intellectual disability may compound the health burden, requiring additional evaluation and management measures. Overall, malformations of greater or lesser severity occur in at least some cases of almost half of the 153 XLID syndromes. Genitourinary abnormalities are most common, but tend to contribute little or no health burden and occur in only a minority of cases of a given XLID syndrome. Some malformations (e.g., lissencephaly, hydranencephaly, long bone deficiency, renal agenesis/dysplasia) are not amenable to medical or surgical intervention; others (e.g., hydrocephaly, facial clefting, cardiac malformations, hypospadias) may be substantially corrected.
© 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  X chromosome; X-linked intellectual disability; birth defects; malformations

Mesh:

Year:  2013        PMID: 24166814      PMCID: PMC3813298          DOI: 10.1002/ajmg.a.36179

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


  24 in total

1.  X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3.

Authors:  L E Siderius; B C Hamel; H van Bokhoven; F de Jager; B van den Helm; H Kremer; J A Heineman-de Boer; H H Ropers; E C Mariman
Journal:  Am J Med Genet       Date:  1999-07-30

2.  Mutations in the chromatin-associated protein ATRX.

Authors:  Richard J Gibbons; Takahito Wada; Christopher A Fisher; Nicola Malik; Matthew J Mitson; David P Steensma; Alan Fryer; David R Goudie; Ian D Krantz; Joanne Traeger-Synodinos
Journal:  Hum Mutat       Date:  2008-06       Impact factor: 4.878

3.  Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene.

Authors:  Karen W Gripp; Elizabeth Hopkins; Jennifer J Johnston; Caitlin Krause; William B Dobyns; Leslie G Biesecker
Journal:  Am J Med Genet A       Date:  2011-09-09       Impact factor: 2.802

4.  X-linked mental retardation and-or hydrocephalus.

Authors:  K Fried
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

5.  A missense mutation confirms the L1 defect in X-linked hydrocephalus (HSAS)

Authors:  M Jouet; A Rosenthal; J MacFarlane; S Kenwrick; D Donnai
Journal:  Nat Genet       Date:  1993-08       Impact factor: 38.330

Review 6.  The telecanthus-hypospadias syndrome.

Authors:  C A Stevens; R S Wilroy
Journal:  J Med Genet       Date:  1988-08       Impact factor: 6.318

7.  Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.

Authors:  Kunio Kitamura; Masako Yanazawa; Noriyuki Sugiyama; Hirohito Miura; Akiko Iizuka-Kogo; Masatomo Kusaka; Kayo Omichi; Rika Suzuki; Yuko Kato-Fukui; Kyoko Kamiirisa; Mina Matsuo; Shin-ichi Kamijo; Megumi Kasahara; Hidefumi Yoshioka; Tsutomu Ogata; Takayuki Fukuda; Ikuko Kondo; Mitsuhiro Kato; William B Dobyns; Minesuke Yokoyama; Ken-ichirou Morohashi
Journal:  Nat Genet       Date:  2002-10-15       Impact factor: 38.330

8.  Syndromic form of X-linked mental retardation with marked hypotonia in early life, severe mental handicap, and difficult adult behavior maps to Xp22.

Authors:  Gillian Turner; Agi Gedeon; Bronwyn Kerr; Rachael Bennett; John Mulley; Michael Partington
Journal:  Am J Med Genet A       Date:  2003-03-15       Impact factor: 2.802

9.  The site of a missense mutation in the extracellular Ig or FN domains of L1CAM influences infant mortality and the severity of X linked hydrocephalus.

Authors:  R C Michaelis; Y Z Du; C E Schwartz
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

10.  Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia.

Authors:  Y Saillour; G Zanni; V Des Portes; D Heron; L Guibaud; M T Iba-Zizen; J L Pedespan; K Poirier; L Castelnau; C Julien; C Franconnet; D Bonthron; M E Porteous; J Chelly; T Bienvenu
Journal:  J Med Genet       Date:  2007-07-06       Impact factor: 6.318

View more
  1 in total

1.  Catalytic deficiency of O-GlcNAc transferase leads to X-linked intellectual disability.

Authors:  Veronica M Pravata; Villo Muha; Mehmet Gundogdu; Andrew T Ferenbach; Poonam S Kakade; Vasudha Vandadi; Ariane C Wilmes; Vladimir S Borodkin; Shelagh Joss; Marios P Stavridis; Daan M F van Aalten
Journal:  Proc Natl Acad Sci U S A       Date:  2019-07-11       Impact factor: 11.205

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.