Literature DB >> 3976721

The phenotypic and cytogenetic spectrum of partial trisomy 9.

G N Wilson, A Raj, D Baker.   

Abstract

A new patient with trisomy for the chromosome segment 9pter----q22 is compared to 19 previously reported cases of partial trisomy 9. Manifestations such as microcephaly, prominent nasal root, bulbous nose, and down-turned corners of the mouth are common to patients with trisomic segments extending from 9p21 to 9q13, while intra-uterine growth retardation, cleft lip/palate, skeletal anomalies, and heart defects are more common with trisomic segments extending through 9q22-9q32. A graphic method illustrates this progression in the partial trisomy 9 malformation spectrum as the triplicated chromosome region extends from bands 9p21 to 9q32. More severe and random defects are observed with complete trisomy 9 or tetrasomy 9p, suggesting an extreme excess of material greatly increases developmental variability.

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Mesh:

Year:  1985        PMID: 3976721     DOI: 10.1002/ajmg.1320200211

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


  14 in total

Review 1.  The origin and evolution of vertebrate sex chromosomes and dosage compensation.

Authors:  A M Livernois; J A M Graves; P D Waters
Journal:  Heredity (Edinb)       Date:  2011-11-16       Impact factor: 3.821

2.  Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).

Authors:  B R Haddad; A E Lin; H Wyandt; A Milunsky
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

3.  Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features.

Authors:  A M Estop; P A Mowery-Rushton; K M Cieply; S J Kochmar; C R Sherer; M Clemens; U Surti; E McPherson
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

4.  Molecular genetic analysis of partial 9p trisomy in two Chinese families with mental retardation and facial anomaly.

Authors:  Aiping Feng; Xiaohua Dai; Xiaoran Wang; Yong Gao; Ruili Luo; Yulei Li; Na Zhang; Jingyu Liu
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2011-08-07

5.  De Novo Duplication of Chromosome 9p in a Female Infant: Phenotype and Genotype Correlation.

Authors:  Paola E Leone; Andy Pérez-Villa; Verónica Yumiceba; María Ángeles Hernández; Jennyfer M García-Cárdenas; Isaac Armendáriz-Castillo; Santiago Guerrero; Patricia Guevara-Ramírez; Andrés López-Cortés; Ana Karina Zambrano; Juan Luis García; Jesús María Hernández; César Paz-Y-Miño
Journal:  J Pediatr Genet       Date:  2019-09-16

6.  Dandy-Walker malformations in a case of partial trisomy 9p (p12.1→pter) due to maternal translocation t(9;12)(p12.1;p13.3).

Authors:  Babu Rao Vundinti; Lily Kerketta; Seema Korgaonkar; Kanjaksha Ghosh
Journal:  Indian J Hum Genet       Date:  2007-01

7.  Duplication 9p and their implication to phenotype.

Authors:  Roberta Santos Guilherme; Vera Ayres Meloni; Ana Beatriz Alvarez Perez; Ana Luiza Pilla; Marco Antonio Paula de Ramos; Anelisa Gollo Dantas; Sylvia Satomi Takeno; Leslie Domenici Kulikowski; Maria Isabel Melaragno
Journal:  BMC Med Genet       Date:  2014-12-20       Impact factor: 2.103

Review 8.  De novo 9q gain in an infant with tetralogy of Fallot with absent pulmonary valve: Patient report and review of congenital heart disease in 9q duplication syndrome.

Authors:  Ina E Amarillo; Shawn O'Connor; Caroline K Lee; Marcia Willing; Jennifer A Wambach
Journal:  Am J Med Genet A       Date:  2015-08-19       Impact factor: 2.802

9.  7q36 deletion and 9p22 duplication: effects of a double imbalance.

Authors:  Karla de Oliveira Pelegrino; Sofia Sugayama; Ana Lúcia Catelani; Karina Lezirovitz; Fernando Kok; Maria de Lourdes Chauffaille
Journal:  Mol Cytogenet       Date:  2013-01-15       Impact factor: 2.009

10.  A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): a case report.

Authors:  Yu-Chun Zhou; Cui Zhang; Jin-Sheng Zhai; Tian-Fu Li; Qiu-Yue Wu; Wei-Wei Li; Na Li; Xiao-Jun Li; Yu-Feng Huang; Ying-Xia Cui; Xin-Yi Xia
Journal:  Mol Med Rep       Date:  2015-03-05       Impact factor: 2.952

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