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Guide to prevention & cure of autoimmune diseases, Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) ,
Welcome to CIDP International Foundation . Global Support for medical disorders & CIDP Number-1 in autoimmune diseases Prevention & healing of all diseases. Mission: prevention & reversal of all تمام بیماریوں

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2. What is Apert Syndrome?

Medical information including definition, major and related features of the condition, genetics.

Category:

Conditions and Diseases > Facial Differences > Apert Syndrome

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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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3. Swedish Apert Syndrome Information

General information about Apert syndrome with photographs of people with the condition. English version follows Swedish text.

Category:

Conditions and Diseases > Facial Differences > Apert Syndrome

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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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4. Apert Syndrome

Resource for contacts, chat rooms, pen pals and other relevant links.

Category:

Conditions and Diseases > Facial Differences > Apert Syndrome

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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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5. Apert Syndrome

Frequently asked questions and answers on Apert syndrome.

Category:

Conditions and Diseases > Facial Differences > 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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6. Romberg's Syndrome

General information, contacts, on-line discussion groups and links.

Category:

Conditions and Diseases > Facial Differences > Parry-Rombergs Syndrome

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The Parry Romberg Foundation is a nonprofit organization whose mission is to develop and provide resources for research, advocacy, education, and support for persons with Parry Romberg Syndrome, their families, doctors, and communities. The Foundation will achieve this mission by raising financial
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7. Parry Romberg Syndrome

Stories from people affected by Parry Romberg syndrome, support and information.

Category:

Conditions and Diseases > Facial Differences > Parry-Rombergs Syndrome

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- support group for people with Romberg's. The Canny Link Directory is owned by: Traffic Connection, Inc. "Web Site Marketing Specialists" ©The Canny Link Directory 1997-2010 Largest Hand Coded Directory that was created by one individual. Canny Link is a unique directory that still
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8. Cornelia de Lange Syndrome (CdLS) Foundation Outreach

Family support organization which exists to ensure the early and accurate diagnosis of CdLS, promote research into the causes and manifestations of the syndrome, and help people with a diagnosis of CdLS, and others with similar characteristics, make informed decisions throughout their lifetime.

Category:

Conditions and Diseases > Genetic Disorders

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The Cornelia de Lange Syndrome (CdLS) Foundation is a family support organization that exists to ensure early and accurate diagnosis of CdLS, promote research into the causes and manifestations of the syndrome, and help people with a diagnosis of CdLS make informed decisions throughout their lives. The CdLS Foundation is a national non-profit organization that has served people with CdLS and their families since 1981. The Foundation's mission is reflected in its slogan: Reaching Out, Providing Help, and Giving Hope.
The CdLS Story Bank is a collection of stories from parents, relatives, friends, and caregivers who wish to share their CdLS experience. These stories let others know they are not alone. They also provide inspiration, insight and, at times, a little humor. Cornelia de Lange Syndrome Foundation

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