Congenita Support

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amcsupport

    https://amcsupport.org/
    Arthrogryposis Multiplex Congenita Support, Inc. 2018 Membership Form Nationally recognized as an Official 501 (c)(3) Non-Profit Organization All of our programs are fully funded by our AMC community.

Arthrogryposis Multiplex Congenita Support, Inc.

    https://rarediseases.org/organizations/arthrogryposis-multiplex-congenita-support-inc/
    Description Arthrogryposis Multiplex Congenita Support, Inc. (AMCSI) is a 501(c)(3) voluntary organization whose mission is to provide and encourage more understanding and mutual support among anyone affected with the diagnosis of arthrogryposis multiplex congenita (AMC) and to create a higher standard of AMC awareness by means of conferences, meetings, and studies.

Arthrogryposis multiplex congenita Genetic and Rare ...

    https://rarediseases.info.nih.gov/diseases/777/arthrogryposis
    Jan 12, 2015 · Arthrogryposis Multiplex Congenita Support, Inc offers an information page on Arthrogryposis multiplex congenita. Please click on the link to access this resource. The National Organization for Rare Disorders (NORD) has a report for patients and families about this condition. NORD is a patient advocacy organization for individuals with rare ...

Arthrogryposis Multiplex Congenita Support, Inc.

    https://www.facebook.com/AMCSUPPORT
    #GivingTuesday is a global day of giving fueled by the power of social media and collaboration. Join the movement and give, whether it’s some of your time, a donation, gift or the power of your voice, and help Arthrogryposis Multiplex Congenita Support providing hope for all those affected by AMC.Followers: 12K

Arthrogryposis Multiplex Congenita Support Inc.

    https://rarediseases.info.nih.gov/organizations/425
    Synonyms: DA2B, Arthrogryposis multiplex congenita distal type 2B, Freeman Sheldon syndrome, variant, Arthrogryposis multiplex congenita distal type II with craniofacial abnormalities, Distal arthrogryposis type IIB, Freeman-Sheldon syndrome variant, Freeman Sheldon variant, Distal arthrogryposis type 2B

Arthrogryposis - DisabilityInfo.org

    https://disabilityinfo.org/fact-sheet-library/disabilitiesillnesses/arthrogryposis/
    Apr 12, 2019 · Arthrogryposis (Arthrogryposis Multiplex Congenita) is a term describing the presence of a muscle disorder that causes multiple joint contractures at birth. A contracture is a limitation in the range of motion of a joint. Associations/Groups: AVENUES – Avenues is a support group for arthrogryposis multiplex congenita. Email: info ...

Team Telomere A Community for Telomere Biology Disorders

    https://teamtelomere.org/
    Our Mission A Community of Telomere Biology Disorders. Our mission is to provide information and support services to families worldwide affected by Dyskeratosis Congenita and Telomere Biology Disorders, to encourage the medical community’s research in finding causes and effective treatments, and to facilitate improved diagnosis by educating medical providers.

amcsupport » About Arthrogryposis

    https://amcsupport.org/about-arthrogryposis/
    Arthrogryposis multiplex congenita (AMC), commonly referred to as arthrogryposis, is the medical term describing the presence of multiple congenital contractures. The word arthrogryposis (arthro, from Greek meaning joint, gryp meaning curved, posis meaning fixed) refers to curved joint(s) in a fixed position.

Myotonia congenita - Genetics Home Reference - NIH

    https://ghr.nlm.nih.gov/condition/myotonia-congenita
    Oct 29, 2019 · Myotonia congenita is a disorder that affects muscles used for movement (skeletal muscles).Beginning in childhood, people with this condition experience bouts of sustained muscle tensing (myotonia) that prevent muscles from relaxing normally.

Myotonia congenita - Wikipedia

    https://en.wikipedia.org/wiki/Myotonia_congenita
    Myotonia congenita, is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder. The hallmark of the disease is the failure of initiated contraction to terminate, often referred to as delayed relaxation of the muscles and rigidity. Symptoms ...Causes: Genetic, CLCN1 mutations



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