Literature DB >> 1856838

Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1).

J P Park1, J B Moeschler, S Z Berg, D H Wurster-Hill.   

Abstract

A 28 year old man with mental retardation and therapeutically controlled schizophrenia was found to have a de novo interstitial deletion in the long arm of a chromosome 9 (46,XY,del(9)(q32q34.1). Additional phenotypic abnormalities included short stature, a short webbed neck with a low posterior hairline, dysmorphic facies, a narrow palate with an inverted V soft palate, and tapered fingers with bilateral short fifth metacarpals. Interstitial deletion of chromosome 9 is a rare finding and we are aware of only one other case involving the q32q34.1 region.

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Year:  1991        PMID: 1856838      PMCID: PMC1016835          DOI: 10.1136/jmg.28.4.282

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  3 in total

1.  [Intercalary deletions of 9q].

Authors:  C Turleau; J de Grouchy; J P Chabrolle
Journal:  Ann Genet       Date:  1978-12

2.  De novo interstitial deletion in the long arm of chromosome 9: a new chromosome syndrome.

Authors:  K L Ying; C J Curry; K B Rajani; S H Kassel; R S Sparkes
Journal:  J Med Genet       Date:  1982-02       Impact factor: 6.318

3.  An interstitial deletion of chromosome 9 in a girl with multiple congenital anomalies.

Authors:  L Wisniewski; G Purdy; T Hassold; C Wilson; K Bentley; E Hackel; J V Higgins
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

  3 in total
  6 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.  Chromosomal abnormalities and schizophrenia.

Authors:  A S Bassett; E W Chow; R Weksberg
Journal:  Am J Med Genet       Date:  2000

3.  Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.

Authors:  Tiffany A Greenwood; Laura C Lazzeroni; Adam X Maihofer; Neal R Swerdlow; Monica E Calkins; Robert Freedman; Michael F Green; Gregory A Light; Caroline M Nievergelt; Keith H Nuechterlein; Allen D Radant; Larry J Siever; Jeremy M Silverman; William S Stone; Catherine A Sugar; Debby W Tsuang; Ming T Tsuang; Bruce I Turetsky; Ruben C Gur; Raquel E Gur; David L Braff
Journal:  JAMA Psychiatry       Date:  2019-12-01       Impact factor: 21.596

Review 4.  Chromosome abnormalities, mental retardation and the search for genes in bipolar disorder and schizophrenia.

Authors:  D H R Blackwood; T Thiagarajah; P Malloy; B S Pickard; W J Muir
Journal:  Neurotox Res       Date:  2008-10       Impact factor: 3.911

5.  Disruption of the neuronal PAS3 gene in a family affected with schizophrenia.

Authors:  D Kamnasaran; W J Muir; M A Ferguson-Smith; D W Cox
Journal:  J Med Genet       Date:  2003-05       Impact factor: 6.318

6.  A novel familial 9q31.2q32 microdeletion: Muscle cramping, somnolence, fatigue, sensorineural hearing loss, pubertal delay, and short stature.

Authors:  Anand K Ramineni; Trent Burgess; Penny Cruickshanks; David Coman
Journal:  Clin Case Rep       Date:  2019-01-07
  6 in total

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