What is apert syndrome?

Answer:
a genetic disease in which the seams between the skull bones, feet, and hands close earlier than normal. this affects the shape of the head, feet, and hands.
First answer by ID2903204905. Last edit by ID2903204905. Question popularity: 1 [recommend question].

Can you answer these Conditions and Diseases questions?

What parts is found in some viruses? Answer it!
What is not found in a virus? Answer it!
What are the symptoms and causes for pain in lower right abdomen? Answer it!
Can you nurse with food poisoning? Answer it!
How does gene therapy help people with genetic diseases? Answer it!

Relevant answers:

  • How do you get Apert syndrome?

    Apert syndrome is a genetic defect, so that means that the child will have it from conception (it's an autosomal dominant genetic defect, which means that only one parent needs to supply the...

  • How is Apert syndrome diagnosed?

    The characteristics of individuals with Aperts syndrome have the webbing of fingers and toes, or possibly, a cranial malformation, This webbing is caused by apoptosis, which is selective cell death,...

  • What are the implications for apert syndrome?

    Sporadic craniostenosis with oxycephaly and syndactyle sometimes polydactyle hands and feet often with blindness or visual impairment with proptosis and ophthalmoplegia..{taken from dictionary of...

  • Is Apert's syndrome a genetic disorder?

    Yes Apert Syndrome is genetic. I think its autosomal dominant. Any dominant genetic trait or genetic disorder only one parent is needed to pass it down.

  • Is apert syndrome dominant or recessive?

    Recessive, but dominant in some rare cases.

Home

Answer these

How do you get onto Obelisks island on horse isle 2?
In: Computer, Online, and Video Games
Answer it!
What were early Australian clothes made of?
In: Clothing
Answer it!
What are the benefits that you can get from knowing how to sew?
In: Home & Garden
Answer it!
When are The Wanted coming to Japan?
In: Music
Answer it!
» more

Featured guides

» More