Literature DB >> 30976276

Genetic Causes of Craniosynostosis: An Update.

Jacqueline A C Goos1, Irene M J Mathijssen1.   

Abstract

In 1993, Jabs et al. were the first to describe a genetic origin of craniosynostosis. Since this discovery, the genetic causes of the most common syndromes have been described. In 2015, a total of 57 human genes were reported for which there had been evidence that mutations were causally related to craniosynostosis. Facilitated by rapid technological developments, many others have been identified since then. Reviewing the literature, we characterize the most common craniosynostosis syndromes followed by a description of the novel causes that were identified between January 2015 and December 2017.

Entities:  

Keywords:  Calvarial suture development; Chromosomal rearrangement; Common craniosynostosis syndromes; Single-gene causes

Year:  2018        PMID: 30976276      PMCID: PMC6422124          DOI: 10.1159/000492266

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  17 in total

1.  Chiari I malformation in defined genetic syndromes in children: are there common pathways?

Authors:  Veronica Saletti; Ilaria Viganò; Giulia Melloni; Chiara Pantaleoni; Ignazio Gaspare Vetrano; Laura Grazia Valentini
Journal:  Childs Nerv Syst       Date:  2019-07-30       Impact factor: 1.475

2.  The Expanding Phenotypic Spectrum of NUP188 Variants Points Toward Multiple Biological Pathways.

Authors:  Martin Poot
Journal:  Mol Syndromol       Date:  2022-07-06

3.  A dysmorphic mouse model reveals developmental interactions of chondrocranium and dermatocranium.

Authors:  Susan M Motch Perrine; M Kathleen Pitirri; Kazuhiko Kawasaki; Joan T Richtsmeier; Emily L Durham; Mizuho Kawasaki; Hao Zheng; Danny Z Chen
Journal:  Elife       Date:  2022-06-15       Impact factor: 8.713

4.  The developing mouse coronal suture at single-cell resolution.

Authors:  D'Juan T Farmer; Hana Mlcochova; Yan Zhou; Nils Koelling; Guanlin Wang; Neil Ashley; Helena Bugacov; Hung-Jhen Chen; Riana Parvez; Kuo-Chang Tseng; Amy E Merrill; Robert E Maxson; Andrew O M Wilkie; J Gage Crump; Stephen R F Twigg
Journal:  Nat Commun       Date:  2021-08-10       Impact factor: 17.694

5.  Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis.

Authors:  Elin Tønne; Bernt Johan Due-Tønnessen; Inger-Lise Mero; Ulrikke Straume Wiig; Mari Ann Kulseth; Magnus Dehli Vigeland; Ying Sheng; Charlotte von der Lippe; Kristian Tveten; Torstein Ragnar Meling; Eirik Helseth; Ketil Riddervold Heimdal
Journal:  Eur J Hum Genet       Date:  2020-12-07       Impact factor: 4.246

6.  RAB23 coordinates early osteogenesis by repressing FGF10-pERK1/2 and GLI1.

Authors:  Md Rakibul Hasan; Maarit Takatalo; Hongqiang Ma; Ritva Rice; Tuija Mustonen; David Pc Rice
Journal:  Elife       Date:  2020-07-14       Impact factor: 8.140

7.  Clinical and Genetic Characterization of Craniosynostosis in Saudi Arabia.

Authors:  Malak Alghamdi; Taghreed R Alhumsi; Ikhlass Altweijri; Waleed H Alkhamis; Omar Barasain; Kelly J Cardona-Londoño; Reshmi Ramakrishnan; Francisco J Guzmán-Vega; Stefan T Arold; Ghaida Ali; Nouran Adly; Hebatallah Ali; Ahmed Basudan; Muhammed A Bakhrebah
Journal:  Front Pediatr       Date:  2021-04-16       Impact factor: 3.418

Review 8.  Tissue-Nonspecific Alkaline Phosphatase-A Gatekeeper of Physiological Conditions in Health and a Modulator of Biological Environments in Disease.

Authors:  Daniel Liedtke; Christine Hofmann; Franz Jakob; Eva Klopocki; Stephanie Graser
Journal:  Biomolecules       Date:  2020-12-08

9.  Single-cell analysis identifies a key role for Hhip in murine coronal suture development.

Authors:  Greg Holmes; Ana S Gonzalez-Reiche; Madrikha Saturne; Susan M Motch Perrine; Xianxiao Zhou; Ana C Borges; Bhavana Shewale; Joan T Richtsmeier; Bin Zhang; Harm van Bakel; Ethylin Wang Jabs
Journal:  Nat Commun       Date:  2021-12-08       Impact factor: 17.694

10.  Multi-suture craniosynostosis in c.1570C>T (p.Arg524Trp) mutated TRAF7: a case report.

Authors:  Sarut Chaisrisawadisuk; Ajay Taranath; Jonathan Azzopardi; Mark H Moore
Journal:  Childs Nerv Syst       Date:  2021-07-10       Impact factor: 1.475

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