Literature DB >> 17980308

Microcephaly syndromes.

Dianne Abuelo1.   

Abstract

The objective of this article is to review microcephaly from a genetics point of view, especially with regard to the process of identification of syndromes in which small head circumference occurs. Microcephaly can be due to either genetic or environmental causes. It can be the only positive finding or may be part of a syndrome of congenital anomalies. The genetic etiology can be caused by autosomal dominant, autosomal recessive, or X-linked genes or various types of chromosome anomalies. Some of the gene mutations have been identified recently. Syndromic microcephaly is associated with a large number of conditions. Some can be diagnosed, or at least suspected, based on their characteristic facial dysmorphism, and others can be searched for using databases of genetic disorders.

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Year:  2007        PMID: 17980308     DOI: 10.1016/j.spen.2007.07.003

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


  34 in total

1.  Rac1 deficiency in the forebrain results in neural progenitor reduction and microcephaly.

Authors:  Lei Chen; Jaime Melendez; Kenneth Campbell; Chia-Yi Kuan; Yi Zheng
Journal:  Dev Biol       Date:  2008-10-31       Impact factor: 3.582

2.  Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures.

Authors:  Xiaochang Zhang; Jiqiang Ling; Giulia Barcia; Lili Jing; Jiang Wu; Brenda J Barry; Ganeshwaran H Mochida; R Sean Hill; Jill M Weimer; Quinn Stein; Annapurna Poduri; Jennifer N Partlow; Dorothée Ville; Olivier Dulac; Tim W Yu; Anh-Thu N Lam; Sarah Servattalab; Jacqueline Rodriguez; Nathalie Boddaert; Arnold Munnich; Laurence Colleaux; Leonard I Zon; Dieter Söll; Christopher A Walsh; Rima Nabbout
Journal:  Am J Hum Genet       Date:  2014-03-20       Impact factor: 11.025

3.  Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly.

Authors:  Eirini Tsoutsou; Maria Tzetis; Krinio Giannikou; Maria Braoudaki; Anastasis Mitrakos; Stella Amenta; Nikoletta Selenti; Emmanouil Kanavakis; Dimitrios Zafeiriou; Sophia Kitsiou-Tzeli; Helena Fryssira
Journal:  Pediatr Res       Date:  2017-05-24       Impact factor: 3.756

4.  Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4.

Authors:  Duane L Guernsey; Haiyan Jiang; Julie Hussin; Marc Arnold; Khalil Bouyakdan; Scott Perry; Tina Babineau-Sturk; Jill Beis; Nadine Dumas; Susan C Evans; Meghan Ferguson; Makoto Matsuoka; Christine Macgillivray; Mathew Nightingale; Lysanne Patry; Andrea L Rideout; Aidan Thomas; Andrew Orr; Ingrid Hoffmann; Jacques L Michaud; Philip Awadalla; David C Meek; Mark Ludman; Mark E Samuels
Journal:  Am J Hum Genet       Date:  2010-07-09       Impact factor: 11.025

5.  Fetal growth restriction and birth defects with newer and older antiepileptic drugs during pregnancy.

Authors:  Gyri Veiby; Anne Kjersti Daltveit; Bernt A Engelsen; Nils Erik Gilhus
Journal:  J Neurol       Date:  2014-01-22       Impact factor: 4.849

6.  Resuming the obsolete term "small head": when microcephaly occurs without cognitive impairment.

Authors:  Piero Pavone; Andrea D Praticò; Martino Ruggieri; Renata Rizzo; Raffaele Falsaperla
Journal:  Neurol Sci       Date:  2017-07-26       Impact factor: 3.307

7.  Establishing Mouse Models for Zika Virus-induced Neurological Disorders Using Intracerebral Injection Strategies: Embryonic, Neonatal, and Adult.

Authors:  Stephanie A Herrlinger; Qiang Shao; Li Ma; Melinda Brindley; Jian-Fu Chen
Journal:  J Vis Exp       Date:  2018-04-26       Impact factor: 1.355

8.  Association between Zika virus and microcephaly in French Polynesia, 2013-15: a retrospective study.

Authors:  Simon Cauchemez; Marianne Besnard; Priscillia Bompard; Timothée Dub; Prisca Guillemette-Artur; Dominique Eyrolle-Guignot; Henrik Salje; Maria D Van Kerkhove; Véronique Abadie; Catherine Garel; Arnaud Fontanet; Henri-Pierre Mallet
Journal:  Lancet       Date:  2016-03-16       Impact factor: 79.321

9.  Practice parameter: Evaluation of the child with microcephaly (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

Authors:  Stephen Ashwal; David Michelson; Lauren Plawner; William B Dobyns
Journal:  Neurology       Date:  2009-09-15       Impact factor: 9.910

10.  Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.

Authors:  Gabriela E Jones; Pia Ostergaard; Anthony T Moore; Fiona C Connell; Denise Williams; Oliver Quarrell; Angela F Brady; Isabel Spier; Filiz Hazan; Oana Moldovan; Dagmar Wieczorek; Barbara Mikat; Florence Petit; Christine Coubes; Robert A Saul; Glen Brice; Kristiana Gordon; Steve Jeffery; Peter S Mortimer; Pradeep C Vasudevan; Sahar Mansour
Journal:  Eur J Hum Genet       Date:  2013-11-27       Impact factor: 4.246

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