Literature DB >> 1554021

Tissue specificity and stability of mosaicism in Pallister-Killian +i(12p) syndrome: relevance for prenatal diagnosis.

J H Priest1, J M Rust, P M Fernhoff.   

Abstract

We ascertained +i(12p) mosaicism during third trimester in a case of polyhydramnios and diaphragmatic hernia. Primary cultures of amniocytes had colonies with +i(12p), colonies without +i(12p), and mixed colonies with 46/47,+i(12p). The likely explanation was instability and loss of i(12p) during somatic divisions of amniocytes. Fetal blood in third trimester retained +i(12p) in 13% of cells. A review of mosaicism in published cases indicates that factors influencing the presence of +i(12p) include tissue type and in vitro and in vivo age. In blood, amniocyte, and probably bone marrow cultures, +i(12p) is less stable than in fibroblast-like cultures derived from skin and other tissues. Young cultures at early passage are more likely to have +i(12p) than old cultures. Cultures from young (especially fetal) donors are more likely to retain +i(12p) than cultures from adult donors. These rules will be important in determining appropriate tissues for diagnosis and interpretation of mosaicism in this disorder.

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Year:  1992        PMID: 1554021     DOI: 10.1002/ajmg.1320420615

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  9 in total

1.  Mosaicism with a normal cell line and an autosomal structural rearrangement.

Authors:  R J Gardner; H E Dockery; P H Fitzgerald; R G Parfitt; D R Romain; N Scobie; R L Shaw; P Tumewu; A J Watt
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

Review 2.  Cytogenetic analysis in prenatal diagnosis.

Authors:  S A Schonberg
Journal:  West J Med       Date:  1993-09

3.  Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.

Authors:  Laura K Conlin; Brian D Thiel; Carsten G Bonnemann; Livija Medne; Linda M Ernst; Elaine H Zackai; Matthew A Deardorff; Ian D Krantz; Hakon Hakonarson; Nancy B Spinner
Journal:  Hum Mol Genet       Date:  2010-01-06       Impact factor: 6.150

4.  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

5.  Advantages of Array Comparative Genomic Hybridization Using Buccal Swab DNA for Detecting Pallister-Killian Syndrome.

Authors:  Veronica Bertini; Simone Gana; Alessandro Orsini; Alice Bonuccelli; Diego Peroni; Valetto Angelo
Journal:  Ann Lab Med       Date:  2019-03       Impact factor: 3.464

Review 6.  Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime.

Authors:  Lars Anders Forsberg; Devin Absher; Jan Piotr Dumanski
Journal:  J Med Genet       Date:  2012-11-21       Impact factor: 6.318

7.  Republished: Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime.

Authors:  Lars Anders Forsberg; Devin Absher; Jan Piotr Dumanski
Journal:  Postgrad Med J       Date:  2013-07       Impact factor: 2.401

8.  Pallister-Killian syndrome.

Authors:  Aarthi Srinivasan; Debra Wright
Journal:  Am J Case Rep       Date:  2014-05-07

9.  Large Genomic Imbalances in Brugada Syndrome.

Authors:  Irene Mademont-Soler; Mel Lina Pinsach-Abuin; Helena Riuró; Jesus Mates; Alexandra Pérez-Serra; Mònica Coll; José Manuel Porres; Bernat Del Olmo; Anna Iglesias; Elisabet Selga; Ferran Picó; Sara Pagans; Carles Ferrer-Costa; Geòrgia Sarquella-Brugada; Elena Arbelo; Sergi Cesar; Josep Brugada; Óscar Campuzano; Ramon Brugada
Journal:  PLoS One       Date:  2016-09-29       Impact factor: 3.240

  9 in total

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