Molecular causes of primary microcephaly and related diseases: a report from the UNIA Workshop.


Journal

Chromosoma
ISSN: 1432-0886
Titre abrégé: Chromosoma
Pays: Austria
ID NLM: 2985138R

Informations de publication

Date de publication:
06 2020
Historique:
received: 09 05 2020
accepted: 12 05 2020
revised: 09 05 2020
pubmed: 20 5 2020
medline: 10 6 2021
entrez: 20 5 2020
Statut: ppublish

Résumé

The International University of Andalucía (UNIA) Current Trends in Biomedicine Workshop on Molecular Causes of Primary Microcephaly and Related Diseases took place in Baeza, Spain, November 18-20, 2019. This meeting brought together scientists from Europe, the USA and China to discuss recent advances in our molecular and genetic understanding of a group of rare neurodevelopmental diseases characterised by primary microcephaly, a condition in which head circumference is smaller than normal at birth. Microcephaly can be caused by inherited mutations that affect key cellular processes, or environmental exposure to radiation or other toxins. It can also result from viral infection, as exemplified by the recent Zika virus outbreak in South America. Here we summarise a number of the scientific advances presented and topics discussed at the meeting.

Identifiants

pubmed: 32424716
doi: 10.1007/s00412-020-00737-6
pii: 10.1007/s00412-020-00737-6
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

115-120

Auteurs

Travis H Stracker (TH)

Institute for Research in Biomedicine (IRB Barcelona) and Barcelona Institute of Science and Technology, 08028, Barcelona, Spain. travis.stracker@irbbarcelona.org.

Ciaran G Morrison (CG)

Centre for Chromosome Biology, School of Natural Sciences, National University of Ireland Galway, Biosciences Building, Dangan, Galway, H91 TK33, Ireland.

Fanni Gergely (F)

Cancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Robinson Way, Cambridge, CB2 0RE, UK.

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Classifications MeSH