Literature DB >> 21744487

Expanding the clinical and neuroradiological phenotype of 6q27 microdeletion: olfactory bulb aplasia and anosmia.

J C Gerber1, T M Neuhann, N Tyshchenko, M Smitka, K Hackmann.   

Abstract

Subtelomeric deletions of chromosome 6q may result in a syndrome with brain malformations, comprising hydrocephalus and hypoplasia of the corpus callosum. Aplasia of the olfactory bulbs (OB) or anosmia has not been described in this syndrome. We describe a 3-year-old girl and a 25-year-old man with subtelomere 6q deletions. Both patients had aplastic OB and hydrocephalus. Subtelomeric 6q deletions might be underdiagnosed as anosmia can be the only symptom.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21744487     DOI: 10.1002/ajmg.a.34079

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


  8 in total

1.  General olfactory sensitivity database (GOSdb): candidate genes and their genomic variations.

Authors:  Ifat Keydar; Edna Ben-Asher; Ester Feldmesser; Noam Nativ; Arisa Oshimoto; Diego Restrepo; Hiroaki Matsunami; Ming-Shan Chien; Jayant M Pinto; Yoav Gilad; Tsviya Olender; Doron Lancet
Journal:  Hum Mutat       Date:  2012-10-11       Impact factor: 4.878

2.  Spectrum of Clinical and Associated MR Imaging Findings in Children with Olfactory Anomalies.

Authors:  T N Booth; N K Rollins
Journal:  AJNR Am J Neuroradiol       Date:  2016-03-17       Impact factor: 3.825

3.  Genotype-Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature.

Authors:  Xiaolei Xie; Hongyan Chai; Autumn DiAdamo; Brittany Grommisch; Jiadi Wen; Hui Zhang; Peining Li
Journal:  Glob Med Genet       Date:  2022-03-11

4.  Isolated Chromosome 6q27 Terminal Deletion Syndrome.

Authors:  Sabita Bhatta; Marsha Medows; Yogesh Acharya
Journal:  Cureus       Date:  2020-05-13

5.  The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2.

Authors:  Mario Ventura; Claudia R Catacchio; Saba Sajjadian; Laura Vives; Peter H Sudmant; Tomas Marques-Bonet; Tina A Graves; Richard K Wilson; Evan E Eichler
Journal:  Genome Res       Date:  2012-03-14       Impact factor: 9.043

6.  Partial trisomy of chromosome 15q and partial monopsony of 6q due to maternal balanced translocation.

Authors:  Shilpy Singla; Kausik Mandal; Suvasini Sharma; Viswas Chhapola
Journal:  J Pediatr Neurosci       Date:  2014-05

7.  Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter Deletion.

Authors:  Marianna De Cinque; Orazio Palumbo; Ermelinda Mazzucco; Antonella Simone; Pietro Palumbo; Renata Ciavatta; Giuliana Maria; Rosangela Ferese; Stefano Gambardella; Antonella Angiolillo; Massimo Carella; Silvio Garofalo
Journal:  Front Genet       Date:  2017-12-06       Impact factor: 4.599

Review 8.  Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27.

Authors:  Sirisha Peddibhotla; Sandesh C S Nagamani; Ayelet Erez; Jill V Hunter; J Lloyd Holder; Mary E Carlin; Patricia I Bader; Helene M F Perras; Judith E Allanson; Leslie Newman; Gayle Simpson; LaDonna Immken; Erin Powell; Aaron Mohanty; Sung-Hae L Kang; Pawel Stankiewicz; Carlos A Bacino; Weimin Bi; Ankita Patel; Sau W Cheung
Journal:  Eur J Hum Genet       Date:  2014-04-16       Impact factor: 4.246

  8 in total

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