Literature DB >> 14708108

Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation.

Dusica Babovic-Vuksanovic1, S C Jenkins, R Ensenauer, D C Newman, S M Jalal.   

Abstract

Chromosome anomalies are responsible for a significant proportion of patients with mental retardation, and congenital anomalies. Development of new molecular cytogenetic techniques has provided a powerful tool for detection of patients with subtle chromosome abnormalities. Particularly, investigation of the gene-rich subtelomeric regions has generated interest regarding the implications and prevalence of cryptic chromosomal rearrangements. Here we describe an adult with a submicroscopic deletion of 18pter, detected by subtelomeric FISH probe. The patient is a 42-year-old man with a history of developmental delay, moderate mental retardation, and symptoms of paranoid schizophrenia since adolescence. His physical examination is remarkable for only a few dysmorphic findings typically seen in 18p- syndrome (round face, hypertelorism, down-slanted palpebral fissures, temporal narrowing, small hands and feet). He lacks significant short stature, skin changes, and associated anomalies involving internal organs. All known patients with deletions of the short arm of chromosome 18 have either loss of large parts of 18p or of the entire p-arm, or have complex chromosomal rearrangement involving other chromosomes. To our knowledge, this is the first description of a cryptic subtelomeric deletion of 18p and the first case of such a chromosomal anomaly in a patient with schizophrenia. Small subtelomeric chromosomal deletions would be missed by standard G-banded karyotyping. Therefore, FISH analysis using subtelomeric probes should be considered for diagnostic evaluation of patients with psychiatric symptoms and mental retardation in whom the karyotype is normal. Copyright 2003 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2004        PMID: 14708108     DOI: 10.1002/ajmg.a.20391

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  9 in total

1.  Two Distinctively Rare Syndromes in a Case of Primary Amenorrhea: 18p Deletion and Mayer-Rokitansky-Kuster-Hauser Syndromes.

Authors:  Monika Anant; Nutan Raj; Neelu Yadav; Arun Prasad; Subhash Kumar; Ajit K Saxena
Journal:  J Pediatr Genet       Date:  2019-10-30

2.  Neuropsychological function in a child with 18p deletion syndrome: a case report.

Authors:  Brian L Willoughby; Marcus Favero; Ganeshwaran H Mochida; Ellen B Braaten
Journal:  Cogn Behav Neurol       Date:  2014-09       Impact factor: 1.600

3.  Adults with Chromosome 18 Abnormalities.

Authors:  Bridgette Soileau; Minire Hasi; Courtney Sebold; Annice Hill; Louise O'Donnell; Daniel E Hale; Jannine D Cody
Journal:  J Genet Couns       Date:  2014-11-19       Impact factor: 2.537

4.  Patent ductus arteriosus and pulmonary valve stenosis in a patient with 18p deletion syndrome.

Authors:  Chun-Hong Xie; Jian-Bin Yang; Fang-Qi Gong; Zheng-Yan Zhao
Journal:  Yonsei Med J       Date:  2008-06-30       Impact factor: 2.759

5.  Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect.

Authors:  Malgorzata I Srebniak; Marjan Boter; Carla Ma Verboven-Peerden; Gerda Ag Looye-Bruinsma; Gretel Oudesluijs; Robert-Jan H Galjaard; Diane Van Opstal
Journal:  Mol Cytogenet       Date:  2011-12-02       Impact factor: 2.009

6.  A method for accurate detection of genomic microdeletions using real-time quantitative PCR.

Authors:  Rosanna Weksberg; Simon Hughes; Laura Moldovan; Anne S Bassett; Eva W C Chow; Jeremy A Squire
Journal:  BMC Genomics       Date:  2005-12-13       Impact factor: 3.969

7.  Chromosome 18p11.2 harbors susceptibility marker: D18S452, for bipolar affective disorder.

Authors:  Mutahar Andrabi; Arshad Hussain; Fouzia Rashid; Sheikh Ozair Nissar; Idrees Ayoub Shah; Yasir Hasan Rather; Waseem Hassan Ahangar; Nazir Ahmad Dar
Journal:  Indian J Psychiatry       Date:  2013-10       Impact factor: 1.759

8.  A case of 18p deletion syndrome after blepharoplasty.

Authors:  Li-Juan Xu; Lv-Xian Wu; Qing Yuan; Zhi-Gang Lv; Xue-Yan Jiang
Journal:  Int Med Case Rep J       Date:  2017-01-12

Review 9.  Monosomy 18p.

Authors:  Catherine Turleau
Journal:  Orphanet J Rare Dis       Date:  2008-02-19       Impact factor: 4.123

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.