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Apert Syndrome
Medical information including definition, major and related features of the condition, genetics.
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The following was developed from information contained in an article entitled
Clinical Assessment and Multispecialty Management of Apert Syndrome ,
written by Lawrence C. Kaplan, MD, and published in Clinics in Plastic
Surgery-Vol. 18, No. 2, April 1991.
Major Features of Apert Syndrome
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General information about Apert syndrome with photographs of people with the condition. English version follows Swedish text.
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For current information please go to
To live with Aperts syndrome as a child and an adult
Apert's syndrome causes impediments for life:
Apert's syndrome ( acrocephalo syndactyli = high skull plus joined up fingers and toes ) is a summarized name for a number of deformaties in the facial bones,
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Written by her father, this contains biographical detail about living with Apert syndrome.
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Krista was born July 21, 1987. We had no idea that there was any kind of
problem until she was born and, of course, had never heard of Aperts Syndrome.
In addition to the usual problems with the head, fingers and toes Krista
had choanal atresia (bone completely blocking the inside of her nose)
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Resource for contacts, chat rooms, pen pals and other relevant links.
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Apert Support and Information Network
Where to Go to Network with Others
The purpose of the list is to allow us to quickly trade information, through email - questions, answers, news about individual surgeries coming up, surgical or genetic breakthroughs, whatever! Our subscribers include adults
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Frequently asked questions and answers on Apert syndrome.
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Apert Syndrome is a condition involving distortions of the head and face and webbing of
the hands and feet. Characteristics include:
skull - short from back to front, wide on the sides, and overly tall (
eyes - slightly side-spaced, bulging, the eyelids tilt downward abnormally at the sides
face
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A family support network for people affected by Apert syndrome and other craniofacial disorders.
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Hi, hola, kia ora, bonjour, hallo, ciao,
I'm Elizabeth Sears, but all my friends call me Teeter! My
mom and dad made this page for me. If you or someone you
know has Apert Syndrome like me, or if you have any
questions, we would love to hear from you!
This Internet safe haven is dedicated to
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