Literature DB >> 25424979

Mosaicism and clinical genetics.

Nancy B Spinner, Laura K Conlin.   

Abstract

With the introduction of increasingly sensitive technologies for mutation detection such as chromosomal microarrays and next-generation sequencing, the importance of mosaicism for human disease is being more fully appreciated. Mosaicism can occur for any type of mutation, either at the chromosomal or DNA sequence level, and while in many cases mosaicism can modify the clinical effects of a syndrome, there are many alterations that can only occur in mosaic form as the mutation is lethal when present in every cell. Mosaicism can have a wide range of effects, from early pregnancy loss, to organ specific pathology, to modification of clinical syndromes. Recent evidence reveals that generation of mosaic alterations is associated with aging, and our ability to detect mosaic alterations sheds light on normal and pathologic changes across the lifespan.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  Pallister-Killian syndrome; mosaicism; somatic mutation; tissue specific mutation

Mesh:

Year:  2014        PMID: 25424979     DOI: 10.1002/ajmg.c.31421

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  22 in total

1.  Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p Mosaicism.

Authors:  Reha M Toydemir; Emanuele Panza; Maria C Longhurst; Sarah T South; Alan F Rope
Journal:  Mol Syndromol       Date:  2020-04-10

2.  Identification of a novel TBX5 c.755 + 1 G > A variant and related pathogenesis in a family with Holt-Oram syndrome.

Authors:  De-Gang Wang; Xing-Sheng Dong; Yi Xiong; Zhi-Ming Li; Ying-Jun Xie; Shu-Hua Liang; Tian-Hua Huang
Journal:  Am J Med Genet A       Date:  2021-09-06       Impact factor: 2.578

3.  Rare variants in GABRG2 associated with sleep-related hypermotor epilepsy.

Authors:  Jing Han; Shui-Bing Liu; Wen Jiang; Yong-Li Jiang; Chang-Geng Song; Hui-Min Zhou; Ban Feng; Jing-Jing Zhao; Yu Liu; Yu-Lin Man
Journal:  J Neurol       Date:  2022-04-29       Impact factor: 6.682

4.  E1021K Homozygous Mutation in PIK3CD Leads to Activated PI3K-Delta Syndrome 1.

Authors:  Yanping Wang; Xuemei Chen; Qiuyun Yang; Wenjing Tang; Yanjun Jia; Lina Zhou; Yunfei An; Zhiyong Zhang; Xuemei Tang; Xiaodong Zhao
Journal:  J Clin Immunol       Date:  2020-01-17       Impact factor: 8.317

5.  Mosaicism for KCNJ5 Causing Early-Onset Primary Aldosteronism due to Bilateral Adrenocortical Hyperplasia.

Authors:  Andrea G Maria; Mari Suzuki; Annabel Berthon; Crystal Kamilaris; Andrew Demidowich; Justin Lack; Mihail Zilbermint; Fady Hannah-Shmouni; Fabio R Faucz; Constantine A Stratakis
Journal:  Am J Hypertens       Date:  2020-02-22       Impact factor: 3.080

6.  Using Array-Based Comparative Genomic Hybridization to Diagnose Pallister-Killian Syndrome.

Authors:  Mi Na Lee; Jiwon Lee; Hee Joon Yu; Jeehun Lee; Sun Hee Kim
Journal:  Ann Lab Med       Date:  2017-01       Impact factor: 3.464

7.  Papular Epidermal Nevus with "Skyline" Basal Cell Layer Syndrome - Natural Course: Case Report and Literature Review.

Authors:  Carole Anouk Zahn; Peter Itin
Journal:  Case Rep Dermatol       Date:  2017-01-10

8.  Demographic and socioeconomic trends in DNA banking utilization in the USA.

Authors:  Joshua Prudent; Esthermarie Lopez; Donna Dorshorst; Hannah C Cox; Joann N Bodurtha
Journal:  J Community Genet       Date:  2021-06-29

9.  Dental Treatment of a Child with Pallister-Killian Syndrome.

Authors:  Serhan Didinen; Didem Atabek; Gülay Kip; Aslı Patır Münevveroğlu; Özlem Tulunoğlu
Journal:  Case Rep Dent       Date:  2016-02-21

10.  In Utero Exposure to Benzo[a]Pyrene Increases Mutation Burden in the Soma and Sperm of Adult Mice.

Authors:  Matthew J Meier; Jason M O'Brien; Marc A Beal; Beverly Allan; Carole L Yauk; Francesco Marchetti
Journal:  Environ Health Perspect       Date:  2016-07-22       Impact factor: 9.031

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