Molecular causes of primary microcephaly and related diseases: a report from the UNIA Workshop.
Centrosome
Cilia
Congresses as Topic
DNA Damage
DNA Replication
Disease Susceptibility
Genetic Association Studies
Genetic Predisposition to Disease
Genetic Testing
Humans
Microcephaly
/ diagnosis
Neurodevelopmental Disorders
/ diagnosis
Neurogenesis
/ genetics
Phenotype
Spindle Apparatus
/ genetics
Cell fate
Centrosomes
Cilia
DNA damage response
Differentiation
Growth defects
Microcephaly
Mitosis
Neurodevelopment
Stem cells
Journal
Chromosoma
ISSN: 1432-0886
Titre abrégé: Chromosoma
Pays: Austria
ID NLM: 2985138R
Informations de publication
Date de publication:
06 2020
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