Literature DB >> 1605230

Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.

J F Arena1, C Schwartz, R Stevenson, L Lawrence, A Carpenter, R Duara, D Ledbetter, T Huang, T Lehner, J Ott.   

Abstract

We report on a family with X-linked mental retardation (XLMR) and severe spastic paraplegia. Appearance is normal but there is severe involvement of the lower limbs (affected relatives never walked), with minimal involvement of the upper limbs and unusual MRI findings including macrogyria, white matter hypoplasia, lack of myelination and a markedly increased paramagnetic signal suggestive of iron deposition. Linkage studies documented possible linkage, with no recombination, between the disease locus and DXS424. A 7-point linkage analysis yielded a maximum LOD score of 1.9, (theta = 0.00) for three loci spanning Xq22-q25. The combination of the unusual clinical and MRI findings and the tentative localization to a region different than other XLMR syndromes with spastic paraplegia, provide good evidence that this is a new XLMR syndrome.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1605230     DOI: 10.1002/ajmg.1320430172

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


  6 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.  A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25.

Authors:  D A Cabezas; R Slaugh; F Abidi; J F Arena; R E Stevenson; C E Schwartz; H A Lubs
Journal:  J Med Genet       Date:  2000-09       Impact factor: 6.318

3.  X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11.

Authors:  P Strømme; K Sundet; C Mørk; J J Cassiman; J P Fryns; S Claes
Journal:  J Med Genet       Date:  1999-05       Impact factor: 6.318

Review 4.  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

5.  A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients.

Authors:  I Longo; S G M Frints; J-P Fryns; I Meloni; C Pescucci; F Ariani; M Borghgraef; M Raynaud; P Marynen; C Schwartz; A Renieri; G Froyen
Journal:  J Med Genet       Date:  2003-01       Impact factor: 6.318

6.  Characterization of novel isoforms and evaluation of SNF2L/SMARCA1 as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26.

Authors:  Maribeth A Lazzaro; Matthew A M Todd; Paul Lavigne; Dominic Vallee; Adriana De Maria; David J Picketts
Journal:  BMC Med Genet       Date:  2008-02-26       Impact factor: 2.103

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.