Mechanism behind cleft palate development found

jason

Seanchaí
Staff member
Scientists have discovered a new mechanism that explains why a certain gene mutation causes craniofrontonasal syndrome (CFNS), a disorder that causes cleft palate and other malformations in the face, brain, and skeleton.
Previous studies have revealed that a mutation in a gene called ephrin-B1 caused abnormalities in facial development, but researchers were uncertain of how.
Philipe M. Soriano, Professor, Developmental and Regenerative Biology, and Jeffrey O. Bush, PhD, Postdoctoral Fellow, Developmental and Regenerative Biology, both at Mount Sinai School of Medicine, studied mice embryos that were genetically engineered to have a mutation in the ephrin-B1 gene.
They determined that ephrin-B1 controls craniofacial development by signaling cells to multiply and when there is a mutation in this gene, it causes anomalies in the cell proliferation process
"Common thinking has been that ephrin-B1 only guided cells in craniofacial development. We were surprised to learn that, instead, this gene signals for cells to multiply, providing us with a clear understanding of why craniofacial development is abnormal when a mutation is present," said Soriano.


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Eoin

New Member
Now if they could only fix it that would be fantastic! I have a few friends and an aunt who have cleft lips and palates and all of them have had them fixed. But it is terribly embarrassing to some of them anyway.
 
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