Microcephaly is a congenital malformation that leads to a significantly reduced brain size and is often accompanied by developmental delay. An international research team led by Dr. Tran Tuoc from the ...
Mutations in the ASPM gene are the most common cause of primary hereditary microcephaly in humans, a condition characterized by a severely reduced brain size. While ASPM has been studied in rodents ...
Microcephaly is a congenital malformation that leads to a significantly reduced brain size and is often accompanied by developmental delay. An international research team led by Dr. Tran Tuoc from the ...
A consortium of Brazilian research centers has gathered data on 843 children born from 2015 to 2018 with Zika-related ...
CAMPINA GRANDE, Brazil (Reuters) - Ianka Barbosa was 7 months pregnant when she found out her child had microcephaly. Before the baby was even born, the father had gone. Barbosa, 18, blames the ...
Just like pruning a tree helps promote proper growth, the brain uses synaptic pruning to get rid of unnecessary connections between its cells. However, when this normal process, which occurs between ...
Orocraniodigital syndrome (OS), also known as Juberg-Hayward syndrome is a rare autosomal recessive condition. Cleft lip is a common observation in orocraniodigital syndrome. Image Credit: ...
A newly discovered genetic form of neonatal diabetes shows how a single gene defect shuts down insulin production in newborns.
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