Pfeiffer syndrome is a rare condition where a baby’s skull plates join together earlier than ... and developing into independent adults. Types 2 and 3 Pfeiffer syndrome are also treatable, ...

Pfeiffer syndrome happens when the bones in your child’s skull, hands, and feet have fused together too soon in the womb because of a gene mutation. This can cause physical, mental, and internal ...

Pfeiffer syndrome is a rare genetic disorder affecting one in 100,000 people that causes skeletal deformities. People with mild symptoms typically have average lifespans.

If one parent has Pfeiffer syndrome, there is a 50% chance that each child will be born with it. It can also be the result of a new mutation in which neither the mother nor the father is a carrier.

Don’t Google Pfeiffer syndrome, it’s a nightmare.” Pfeiffer syndrome is a rare, genetic disorder in which some skull bones fuse together and grow abnormally, according to the National ...

Pfeiffer syndrome affects about 1 in 100,000 babies, according to the National Institutes of Health, and is caused by a mutation in one of two genes involved in prenatal bone development.