Literature DB >> 21975655

Mosaic trisomy 9 presenting with congenital heart disease, facial dysmorphism and pigmentary skin lesions: intricate issues of genetic counseling.

Siddram J Patil1, Rajitha Ponnala, Sejal Shah, Ashwin Dalal.   

Abstract

Chromosomal mosaicism for full aneuploidy involving chromosome 9 is an uncommon chromosomal abnormality. Mosaic trisomy 9 clinical manifestations are highly variable and difficult to predict. The authors present a case of mosaic trisomy 9 with typical clinical manifestations(facial dysmorphism, various internal organ malformations and severe psychomotor retardation), pigmentary mosaic skin lesions along the lines of Blaschko and evidence of maternal uniparental disomy in skin.

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Year:  2012        PMID: 21975655     DOI: 10.1007/s12098-011-0567-x

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  8 in total

1.  Assessing discrepant findings between QF-PCR on uncultured prenatal samples and karyotyping on long-term culture.

Authors:  Elizabeth T Lau; Linda Tang; Cherry Wong; Lam Yung Hang; A Ghosh; W C Leung; W K Sin; T K Lau; Y Y Kung; Mary H Y Tang
Journal:  Prenat Diagn       Date:  2009-02       Impact factor: 3.050

2.  Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.

Authors:  L Y Hsu; M T Yu; R L Neu; D L Van Dyke; P A Benn; C L Bradshaw; L G Shaffer; R R Higgins; G S Khodr; C C Morton; H Wang; A R Brothman; D Chadwick; C M Disteche; L S Jenkins; D K Kalousek; T J Pantzar; P Wyatt
Journal:  Prenat Diagn       Date:  1997-03       Impact factor: 3.050

3.  A case of maternal uniparental disomy of chromosome 9 diagnosed prenatally and the related problem of residual trisomy.

Authors:  H R Slater; A Ralph; A Daniel; S Worthington; C Roberts
Journal:  Prenat Diagn       Date:  2000-11       Impact factor: 3.050

4.  Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q).

Authors:  E J Björck; B M Anderlid; E Blennow
Journal:  Am J Med Genet       Date:  1999-11-05

Review 5.  Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.

Authors:  I T Thomas; J L Frias; E S Cantu; C Z Lafer; D B Flannery; J G Graham
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

6.  Atypical manifestations of two cases of trisomy 9 syndrome: rethinking development delay.

Authors:  R P Saneto; K E Applegate; D G Frankel
Journal:  Am J Med Genet       Date:  1998-10-30

7.  Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies.

Authors:  L Y Hsu; S Kaffe; E C Jenkins; L Alonso; P A Benn; K David; K Hirschhorn; E Lieber; A Shanske; L R Shapiro
Journal:  Prenat Diagn       Date:  1992-07       Impact factor: 3.050

8.  Mosaic trisomy 9 and lobar holoprosencephaly.

Authors:  Marion Gérard-Blanluet; Claude Danan; Martine Sinico; Françoise Lelong; Elsa Borghi; Gilles Dassieu; Jean-Claude Janaud; Sylvie Odent; Férechté Encha-Razavi
Journal:  Am J Med Genet       Date:  2002-08-15
  8 in total
  4 in total

Review 1.  Trisomy 9 mosaic syndrome: Sixteen additional patients with new and/or less commonly reported features, literature review, and suggested clinical guidelines.

Authors:  Mindy Li; Jennifer Glass; Xiaoli Du; Holly Dubbs; Margaret Horton Harr; Marni Falk; Teresa Smolarek; Robert J Hopkin; Elaine Zackai; Sarah E Sheppard
Journal:  Am J Med Genet A       Date:  2021-05-10       Impact factor: 2.578

Review 2.  Pigmentary mosaicism: a review of original literature and recommendations for future handling.

Authors:  Anna Boye Kromann; Lilian Bomme Ousager; Inas Kamal Mohammad Ali; Nurcan Aydemir; Anette Bygum
Journal:  Orphanet J Rare Dis       Date:  2018-03-05       Impact factor: 4.123

3.  Case report of a pseudo-isodicentric chromosome 9 resulting in mosaic trisomy 9.

Authors:  Sarah M Beaudry; Oleg Shchelochkov; Pamela Trapane; Benjamin Darbro; Jaime M W Nagy
Journal:  Clin Case Rep       Date:  2021-03-09

4.  Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability.

Authors:  Magdalena Bartnik; Beata Nowakowska; Katarzyna Derwińska; Barbara Wiśniowiecka-Kowalnik; Marta Kędzior; Joanna Bernaciak; Kamila Ziemkiewicz; Tomasz Gambin; Maciej Sykulski; Natalia Bezniakow; Lech Korniszewski; Anna Kutkowska-Kaźmierczak; Jakub Klapecki; Krzysztof Szczałuba; Chad A Shaw; Tadeusz Mazurczak; Anna Gambin; Ewa Obersztyn; Ewa Bocian; Paweł Stankiewicz
Journal:  J Appl Genet       Date:  2013-12-03       Impact factor: 3.240

  4 in total

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