Literature DB >> 2248294

Clinical diagnosis of partial duplication 7q.

O Bartsch1, U Kalbe, T K Ngo, R Lettau, E Schwinger.   

Abstract

We report on two sibs with partial dup (7q), a retarded 9-month-old boy and an aborted fetus of 17 weeks' gestational age. Besides minor anomalies, the boy had frontal bossing, macrocephaly with hydrocephaly, a high forehead, and a large fontanelle. GTG banded chromosomes showed a 14p+ abnormality. Because his mother carries a balanced, de novo translocation with a breakpoint in band 7q33, the boy has a duplication of the distal portion of band 7q33 and the segment 7q34----qter. Our findings suggest that the phenotype in terminal duplications of 7q may, in some patients, be recognized clinically.

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Year:  1990        PMID: 2248294     DOI: 10.1002/ajmg.1320370218

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


  8 in total

1.  Tandem duplication of the terminal band of the long arm of chromosome 7 (dir dup (7)(q36----qter)).

Authors:  R S Verma; R A Conte; J H Pitter
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

2.  Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy.

Authors:  U Müller; J L Weber; P Berry; K G Kupke
Journal:  J Med Genet       Date:  1993-07       Impact factor: 6.318

3.  The contribution of 7q33 copy number variations for intellectual disability.

Authors:  Fátima Lopes; Fátima Torres; Sally Ann Lynch; Arminda Jorge; Susana Sousa; João Silva; Paula Rendeiro; Purificação Tavares; Ana Maria Fortuna; Patrícia Maciel
Journal:  Neurogenetics       Date:  2017-12-19       Impact factor: 2.660

4.  Pure Distal 7q Duplication: Describing a Macrocephalic Neurodevelopmental Syndrome, Case Report and Review of the Literature.

Authors:  Kerri Bosfield; Jullianne Diaz; Eyby Leon
Journal:  Mol Syndromol       Date:  2021-03-29

5.  Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome.

Authors:  K Y Gandelman; L Gibson; M S Meyn; T L Yang-Feng
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

6.  Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report.

Authors:  Bárbara Marques; Cristina Ferreira; Filomena Brito; Sónia Pedro; Cristina Alves; Teresa Lourenço; Marta Amorim; Hildeberto Correia
Journal:  Mol Cytogenet       Date:  2016-11-25       Impact factor: 2.009

7.  Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes.

Authors:  Muhammad M Rahman; Km Furkan Uddin; Nesreen K Al Jezawi; Noushad Karuvantevida; Hosneara Akter; Nushrat J Dity; Md Ashiquir Rahaman; Maksuda Begum; Md Atikur Rahaman; Md Abdul Baqui; Zeena Salwa; Serajul Islam; Marc Woodbury-Smith; Mohammed Basiruzzaman; Mohammed Uddin
Journal:  Mol Genet Genomic Med       Date:  2019-09-01       Impact factor: 2.183

8.  Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report.

Authors:  Felipe Ruiz-Botero; Harry Pachajoa
Journal:  J Med Case Rep       Date:  2016-07-27
  8 in total

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