Literature DB >> 1746601

New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.

M Wilson1, J Mulley, A Gedeon, H Robinson, G Turner.   

Abstract

We describe 14 males from 3 successive generations in a family who have X-linked mental retardation (XLMR), obesity, gynecomastia, speech difficulties, emotional lability, tapering fingers, and small feet. Linkage analysis using markers spread along the X chromosome demonstrated a gene localisation close to the centromere. Maximum lod scores for markers near the centromere, all at theta = 0.00, were 1.36 for DXS72, and 1.46 for DXYS1. The closest flanking markers which showed recombination were DXS84 and DXS94, defining the physical localisation within Xp21.1-q22. DXS255 was fully informative with lod-1 confidence interval for theta of 0.00-0.12. Clinical findings and linkage data in this family distinguish it from the Börjeson-Forssman-Lehmann syndrome and other previously described XLMR syndromes.

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Year:  1991        PMID: 1746601     DOI: 10.1002/ajmg.1320400405

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


  9 in total

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

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5.  A 47, XXY patient and Xq21.31 duplication with features of Prader-Willi syndrome: results of array-based comparative genomic hybridization.

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7.  X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism.

Authors:  H G Brunner; M R Nelen; P van Zandvoort; N G Abeling; A H van Gennip; E C Wolters; M A Kuiper; H H Ropers; B A van Oost
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  9 in total

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