Literature DB >> 9111997

Clinical variability of tetrasomy 12p.

G B Schaefer1, A Jochar, R Muneer, W G Sanger.   

Abstract

We describe five patients with tetrasomy 12p (one previously reported). These patients exhibit a very wide range of phenotypic features from that of classic Pallister-Killian syndrome to only mild learning disabilities with pigmentary skin changes. As such, these cases highlight the fact that tetrasomy 12p [i(12p)] and Pallister-Killian syndrome are not synonymous, although this combination of genotype and phenotype is often seen. This information is especially important in prenatally ascertained i(12p). The full spectrum of phenotypic possibilities associated with this chromosome aneuploidy should be discussed in prenatal counseling.

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Year:  1997        PMID: 9111997     DOI: 10.1111/j.1399-0004.1997.tb02429.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  8 in total

Review 1.  Congenital diaphragmatic hernia and associated cardiovascular malformations: type, frequency, and impact on management.

Authors:  Angela E Lin; Barbara R Pober; Ian Adatia
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-05-15       Impact factor: 3.908

2.  The Pallister-Killian syndrome in a child with rare karyotype--a diagnostic problem.

Authors:  Robert Smigiel; Jacek Pilch; Izabela Makowska; Halina Busza; Ryszard Slezak; Maria M Sasiadek
Journal:  Eur J Pediatr       Date:  2007-11-14       Impact factor: 3.183

Review 3.  Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH.

Authors:  Barbara R Pober
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-05-15       Impact factor: 3.908

Review 4.  Neuroimaging findings in Pallister-Killian syndrome.

Authors:  Emil Jernstedt Barkovich; Tarannum Musvee Lateef; Matthew T Whitehead
Journal:  Neuroradiol J       Date:  2017-12-20

Review 5.  Genetic aspects of human congenital diaphragmatic hernia.

Authors:  B R Pober
Journal:  Clin Genet       Date:  2008-05-28       Impact factor: 4.438

6.  Cognitive, Behavioral, and Sensory Profile of Pallister-Killian Syndrome: A Prospective Study of 22 Individuals.

Authors:  Anna Fetta; Luca Soliani; Alessia Trevisan; Rosa Pugliano; Emilia Ricci; Veronica Di Pisa; Veronica Pignataro; Marida Angotti; Alessandro Rocca; Bianca Salce; Maria Margherita Mancardi; Lucio Giordano; Dario Pruna; Antonia Parmeggiani; Duccio Maria Cordelli
Journal:  Genes (Basel)       Date:  2022-02-16       Impact factor: 4.096

7.  Case Report: A Case Study on the Neurodevelopmental Profile of a Child With Pallister-Killian Syndrome and His Unaffected Twin.

Authors:  Carole A Samango-Sprouse; Mary P Hamzik; Kenneth Rosenbaum; Kosar Khaksari; Francie Mitchell; Ritika Kommareddi; Michaela R Brooks; Elizabeth Tipton; Teresa Sadeghin; Andrea L Gropman
Journal:  Front Pediatr       Date:  2022-03-15       Impact factor: 3.418

8.  Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases.

Authors:  Birsen Karaman; Hülya Kayserili; Asadollah Ghanbari; Zehra Oya Uyguner; Güven Toksoy; Umut Altunoglu; Seher Basaran
Journal:  Mol Cytogenet       Date:  2018-08-17       Impact factor: 2.009

  8 in total

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