Literature DB >> 1583663

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

R S Verma1, R A Conte, J H Pitter.   

Abstract

We report on a new case of a single band duplication of the long arm of chromosome 7, dir dup (7)(q36----qter). The major manifestations are developmental delay (particularly speech), frontal bossing, macrocrania, and constant drooling. When compared with other cases involving a 7q duplication of various segments, our patient has a few minor anomalies. This case illustrates the genotype/phenotype correlation in a child with a single band duplication which has resulted in duplication of 7q36----qter. A tabulation of reported cases with duplication of various segments of 7q is provided, which may serve as an aid for clinicians.

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Mesh:

Year:  1992        PMID: 1583663      PMCID: PMC1015957          DOI: 10.1136/jmg.29.5.344

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  4 in total

1.  The phenotype of partial dup(7q) reconsidered: a report of five new cases.

Authors:  A Forabosco; A Baroncini; L Dalpra; L Chessa; A Giannotti; F Maccagnani; B Dallapiccola
Journal:  Clin Genet       Date:  1988-07       Impact factor: 4.438

2.  Partial trisomy for the long arm of chromosome 7. Case report and review.

Authors:  M A Novales; C Fernandez-Novoa; A Hevia; V San Martin; H Galera
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  Clinical diagnosis of partial duplication 7q.

Authors:  O Bartsch; U Kalbe; T K Ngo; R Lettau; E Schwinger
Journal:  Am J Med Genet       Date:  1990-10

4.  Full trisomy 7 and Potter syndrome.

Authors:  E Yunis; E Ramírez; J G Uribe
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  4 in total
  8 in total

1.  A rare chromosomal abnormality inherited from the mother in a boy conceived after intracytoplasmic sperm injection: a case report.

Authors:  Li Yin; Hong Tian; Long-jie Gu; Ding Ma; Han-wang Zhang; Gui-jin Zhu
Journal:  J Assist Reprod Genet       Date:  2012-05-24       Impact factor: 3.412

2.  17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD).

Authors:  Christine M Armour; Dennis E Bulman; Olga Jarinova; Richard Curtis Rogers; Kate B Clarkson; Barbara R DuPont; Alka Dwivedi; Frank O Bartel; Laura McDonell; Charles E Schwartz; Kym M Boycott; David B Everman; Gail E Graham
Journal:  Eur J Hum Genet       Date:  2011-06-01       Impact factor: 4.246

3.  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

4.  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

5.  Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3.

Authors:  Asayeon Choi; Ja-Young Oh; Myungshin Kim; Woori Jang; Dae-Hyun Jang
Journal:  Ann Rehabil Med       Date:  2017-10-31

6.  4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report.

Authors:  Maolan Wu; Xiangrong Zheng; Xia Wang; Guoyuan Zhang; Jian Kuang
Journal:  BMC Med Genomics       Date:  2020-03-03       Impact factor: 3.063

7.  A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics.

Authors:  Aihua Yin; Jian Lu; Chang Liu; Li Guo; Jing Wu; Mingqin Mai; Yanfang Zhong; Xiaozhuang Zhang
Journal:  Mol Cytogenet       Date:  2014-04-15       Impact factor: 2.009

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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