Literature DB >> 26235846

5p deletions: Current knowledge and future directions.

Joanne M Nguyen, Krista J Qualmann, Rebecca Okashah, AmySue Reilly, Mikhail F Alexeyev, Dennis J Campbell.   

Abstract

Disorders resulting from 5p deletions (5p-) were first recognized by Lejeune et al. in 1963 [Lejeune et al. (1963); C R Hebd Seances Acad Sci 257:3098-3102]. 5p- is caused by partial or total deletion of the short arm of chromosome 5. The most recognizable phenotype is characterized by a high-pitched cry, dysmorphic features, poor growth, and developmental delay. This report reviews 5p- disorders and their molecular basis. Hemizygosity for genes located within this region have been implicated in contributing to the phenotype. A review of the genes on 5p which may be dosage sensitive is summarized. Because of the growing knowledge of these specific genes, future directions to explore potential targeted therapies for individuals with 5p- are discussed.
© 2015 Wiley Periodicals, Inc. © 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  5p deletion syndrome; 5p minus syndrome; Cri du Chat syndrome; haploinsufficiency; hemizygosity; natural history

Mesh:

Year:  2015        PMID: 26235846      PMCID: PMC4736720          DOI: 10.1002/ajmg.c.31444

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  115 in total

Review 1.  Protein transduction: an alternative to genetic intervention?

Authors:  K G Ford; B E Souberbielle; D Darling; F Farzaneh
Journal:  Gene Ther       Date:  2001-01       Impact factor: 5.250

2.  Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion.

Authors:  J-S Fang; K-F Lee; C-T Huang; C-L Syu; K-J Yang; L-H Wang; D-L Liao; C-H Chen
Journal:  Clin Genet       Date:  2008-04-08       Impact factor: 4.438

3.  Receptive and expressive language skills in children with cri-du-chat syndrome.

Authors:  K M Cornish; F Munir
Journal:  J Commun Disord       Date:  1998 Jan-Feb       Impact factor: 2.288

4.  Five novel genes from the cri-du-chat critical region isolated by direct selection.

Authors:  A D Simmons; S A Goodart; T D Gallardo; J Overhauser; M Lovett
Journal:  Hum Mol Genet       Date:  1995-02       Impact factor: 6.150

5.  Amelioration of the typical cognitive phenotype in a patient with the 5pter deletion associated with Cri-du-chat syndrome in addition to a partial duplication of CTNND2.

Authors:  Jennifer M Sardina; Allyson R Walters; Kathryn E Singh; Renius X Owen; Virginia E Kimonis
Journal:  Am J Med Genet A       Date:  2014-03-26       Impact factor: 2.802

Review 6.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

Review 7.  Histone deacetylase inhibitors: therapeutic agents and research tools for deciphering motor neuron diseases.

Authors:  A Echaniz-Laguna; O Bousiges; J-P Loeffler; A-L Boutillier
Journal:  Curr Med Chem       Date:  2008       Impact factor: 4.530

8.  Evidence for a distinct region causing a cat-like cry in patients with 5p deletions.

Authors:  M Gersh; S A Goodart; L M Pasztor; D J Harris; L Weiss; J Overhauser
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

9.  Barrier mechanisms in the developing brain.

Authors:  Norman R Saunders; Shane A Liddelow; Katarzyna M Dziegielewska
Journal:  Front Pharmacol       Date:  2012-03-29       Impact factor: 5.810

Review 10.  Cri du Chat syndrome.

Authors:  Paola Cerruti Mainardi
Journal:  Orphanet J Rare Dis       Date:  2006-09-05       Impact factor: 4.123

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  18 in total

Review 1.  Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

Authors:  Mary Ella Pierpont; Martina Brueckner; Wendy K Chung; Vidu Garg; Ronald V Lacro; Amy L McGuire; Seema Mital; James R Priest; William T Pu; Amy Roberts; Stephanie M Ware; Bruce D Gelb; Mark W Russell
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

2.  Novel rearrangements between different chromosomes with direct impact on the diagnosis of 5p- syndrome.

Authors:  Samar Nasser Chehimi; Vanessa Tavares Almeida; Amom Mendes Nascimento; Évelin Aline Zanardo; Yanca Gasparini de Oliveira; Gleyson Francisco da Silva Carvalho; Beatriz Martins Wolff; Marilia Moreira Montenegro; Nilson Antônio de Assunção; Chong Ae Kim; Leslie Domenici Kulikowski
Journal:  Clinics (Sao Paulo)       Date:  2022-05-28       Impact factor: 2.898

3.  Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohort.

Authors:  Nasna Nassir; Isra Sati; Shaiban Al Shaibani; Awab Ahmed; Omar Almidani; Hosneara Akter; Marc Woodbury-Smith; Ahmad Abou Tayoun; Mohammed Uddin; Ammar Albanna
Journal:  Neurogenetics       Date:  2022-03-24       Impact factor: 2.660

4.  Genetic Basis of Human Congenital Heart Disease.

Authors:  Shannon N Nees; Wendy K Chung
Journal:  Cold Spring Harb Perspect Biol       Date:  2020-09-01       Impact factor: 9.708

5.  Ebstein anomaly associated with cri du chat (cat's cry) syndrome and 20q duplication.

Authors:  Alberto Olivella; Hernan Manotas; César Payán-Gómez; Juan Gabriel Piñeros
Journal:  BMJ Case Rep       Date:  2020-06-01

6.  Neoplasia in Cri du Chat Syndrome from Italian and German Databases.

Authors:  Andrea Guala; Marianna Spunton; Silvia Kalantari; Ingo Kennerknecht; Cesare Danesino
Journal:  Case Rep Genet       Date:  2017-04-24

7.  Difficult airway management and suspected malignant hyperthermia in a Child with Cri Du Chat Syndrome.

Authors:  Andrew O Amata
Journal:  Saudi J Anaesth       Date:  2019 Jan-Mar

8.  Cri-du-chat syndrome mimics Silver-Russell syndrome depending on the size of the deletion: a case report.

Authors:  Yerai Vado; Javier Errea-Dorronsoro; Isabel Llano-Rivas; Nerea Gorria; Arrate Pereda; Blanca Gener; Laura Garcia-Naveda; Guiomar Perez de Nanclares
Journal:  BMC Med Genomics       Date:  2018-12-27       Impact factor: 3.063

9.  Cri-Du-Chat Syndrome: Clinical Profile and Chromosomal Microarray Analysis in Six Patients.

Authors:  Layla Damasceno Espirito Santo; Lília Maria Azevedo Moreira; Mariluce Riegel
Journal:  Biomed Res Int       Date:  2016-04-07       Impact factor: 3.411

10.  Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics.

Authors:  Emiy Yokoyama; Victoria Del Castillo; Silvia Sánchez; Sandra Ramos; Bertha Molina; Leda Torres; María José Navarro; Silvia Avila; José Luis Castrillo; Benilde García-De Teresa; Bárbara Asch; Sara Frías
Journal:  Mol Cytogenet       Date:  2018-05-09       Impact factor: 2.009

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