Literature DB >> 8456840

New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death.

K H Gustavson1, G Annerén, H Malmgren, N Dahl, C G Ljunggren, H Bäckman.   

Abstract

A family with an X-linked mental retardation syndrome involving seven children in two generations is reported. The syndrome includes microcephaly, severe mental retardation, optic atrophy with severely impaired vision or blindness, a severe hearing defect, spasticity, epileptic seizures, restricted movement of the large joints, and death in infancy or early childhood. We conclude that this is a distinct, previously unrecognized X-linked mental retardation syndrome.

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Year:  1993        PMID: 8456840     DOI: 10.1002/ajmg.1320450527

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  10 in total

1.  X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.

Authors:  A L Christianson; R E Stevenson; C H van der Meyden; J Pelser; F W Theron; P L van Rensburg; M Chandler; C E Schwartz
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

2.  X-linked mental retardation: in pursuit of a gene map.

Authors:  C E Schwartz
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

3.  Linkage mapping of a severe X-linked mental retardation syndrome.

Authors:  H Malmgren; M Sundvall; N Dahl; K H Gustavson; G Annerén; C Wadelius; M L Steén-Bondeson; U Pettersson
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

4.  A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.

Authors:  V Shashi; M N Berry; S Shoaf; J J Sciote; D Goldstein; T C Hart
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

5.  A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

Authors:  L Tranebjaerg; C Schwartz; H Eriksen; S Andreasson; V Ponjavic; A Dahl; R E Stevenson; M May; F Arena; D Barker
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

6.  Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26.

Authors:  H G Yntema; B C Hamel; A P Smits; T van Roosmalen; B van den Helm; H Kremer; H H Ropers; D F Smeets; H van Bokhoven
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

Review 7.  X-linked disorders with cerebellar dysgenesis.

Authors:  Ginevra Zanni; Enrico S Bertini
Journal:  Orphanet J Rare Dis       Date:  2011-05-15       Impact factor: 4.123

8.  Human teneurin-1 is a direct target of the homeobox transcription factor EMX2 at a novel alternate promoter.

Authors:  Jan Beckmann; Antonio Vitobello; Jacqueline Ferralli; Daniela Kenzelmann Brož; Filippo M Rijli; Ruth Chiquet-Ehrismann
Journal:  BMC Dev Biol       Date:  2011-06-08       Impact factor: 1.978

Review 9.  On the Teneurin track: a new synaptic organization molecule emerges.

Authors:  Timothy J Mosca
Journal:  Front Cell Neurosci       Date:  2015-05-27       Impact factor: 5.505

10.  Loss of ARHGEF6 Causes Hair Cell Stereocilia Deficits and Hearing Loss in Mice.

Authors:  Chengwen Zhu; Cheng Cheng; Yanfei Wang; Waqas Muhammad; Shuang Liu; Weijie Zhu; Buwei Shao; Zhong Zhang; Xiaoqian Yan; Qingqing He; Zhengrong Xu; Chenjie Yu; Xiaoyun Qian; Ling Lu; Shasha Zhang; Yuan Zhang; Wei Xiong; Xia Gao; Zhigang Xu; Renjie Chai
Journal:  Front Mol Neurosci       Date:  2018-10-02       Impact factor: 5.639

  10 in total

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