Literature DB >> 18947005

Terminal deletion of chromosome 6q.

Pen-Hua Su1, Jia-Yuh Chen, Suh-Jen Chen, Kai-Chi Yang.   

Abstract

Terminal deletions of chromosome 6q are rare. Clinical features associated with 6q terminal deletion syndrome include psychomotor retardation, seizures, hypotonia, short neck, and facial abnormalities, as well as various case-specific anomalies. Here, we describe a girl with 6q terminal deletion syndrome and unusually short stature. Features of previously described patients are also summarized.

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Year:  2008        PMID: 18947005     DOI: 10.1016/S1875-9572(08)60019-4

Source DB:  PubMed          Journal:  Pediatr Neonatol        ISSN: 1875-9572            Impact factor:   2.083


  5 in total

1.  Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay.

Authors:  Giulia Parmeggiani; Stefania Bigoni; Barbara Buldrini; Giampaolo Garani; Luigi Clauser; Manilo Galiè; Alessandra Ferlini; Sergio Fini
Journal:  Mol Syndromol       Date:  2017-09-13

2.  Roles of A-kinase Anchor Protein 12 in Astrocyte and Oligodendrocyte Precursor Cell in Postnatal Corpus Callosum.

Authors:  Hajime Takase; Gen Hamanaka; Ryo Ohtomo; Ji Hyun Park; Kelly K Chung; Irwin H Gelman; Kyu-Won Kim; Josephine Lok; Eng H Lo; Ken Arai
Journal:  Stem Cell Rev Rep       Date:  2021-01-25       Impact factor: 6.692

3.  Genome-Wide Copy Number Variation Association Study of Atrial Fibrillation Related Thromboembolic Stroke.

Authors:  Chia-Shan Hsieh; Pang-Shuo Huang; Sheng-Nan Chang; Cho-Kai Wu; Juey-Jen Hwang; Eric Y Chuang; Chia-Ti Tsai
Journal:  J Clin Med       Date:  2019-03-09       Impact factor: 4.241

4.  A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short-lived infant.

Authors:  María Guadalupe Domínguez; Horacio Rivera; Rosa María Dávalos-Pulido; Ingrid Patricia Dávalos-Rodríguez
Journal:  J Clin Lab Anal       Date:  2020-05-12       Impact factor: 2.352

Review 5.  A child with intellectual disability and dysmorphism due to complex ring chromosome 6: identification of molecular mechanism with review of literature.

Authors:  Frenny Sheth; Thomas Liehr; Viraj Shah; Hillary Shah; Stuti Tewari; Dhaval Solanki; Sunil Trivedi; Jayesh Sheth
Journal:  Ital J Pediatr       Date:  2018-10-11       Impact factor: 2.638

  5 in total

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