Literature DB >> 3625766

Coffin-Lowry syndrome and schizophrenia: a family report.

R A Collacott, J S Warrington, I D Young.   

Abstract

A family is reported in which the mother and 4 of her 6 children are affected by a constellation of abnormalities including mental handicap, abnormal facies, short stature, soft fleshy hands with tapering fingers and skeletal abnormalities. The family is believed to represent a further group of individuals with Coffin-Lowry syndrome. Additionally, one affected daughter has symptoms suggestive of schizophrenia and one affected son has severe sensorineural deafness.

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Year:  1987        PMID: 3625766     DOI: 10.1111/j.1365-2788.1987.tb01356.x

Source DB:  PubMed          Journal:  J Ment Defic Res        ISSN: 0022-264X


  4 in total

1.  Are advanced paternal age and point mutation at chromosome 4 associated with schizophrenia?

Authors:  Vivek H Phutane; Santosh Loganathan; Om P Jhirwal; Mathew Varghese; Sanjeev Jain; Satish C Girimaji
Journal:  Prim Care Companion J Clin Psychiatry       Date:  2010

Review 2.  The Coffin-Lowry syndrome.

Authors:  I D Young
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

3.  Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.

Authors:  V Biancalana; M L Briard; A David; S Gilgenkrantz; J Kaplan; M Mathieu; C Piussan; J Poncin; A Schinzel; C Oudet
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

Review 4.  Coffin-Lowry syndrome: clinical and molecular features.

Authors:  A Hanauer; I D Young
Journal:  J Med Genet       Date:  2002-10       Impact factor: 6.318

  4 in total

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