Digeorge Syndrome Support Network

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22q Support Groups Links 22q Family Foundation

    https://22qfamilyfoundation.org/living-22q/22q-support-groups-links
    for individuals with 22q 11.2 deletion syndrome. Our mission is to connect families and individuals affected by 22q (Velo-Cardio-Facial syndrome, DiGeorge Syndrome) and related disorders. Our son Jonah was diagnosed with 22q 11.2 deletion syndrome when he was 21 months old and is our inspiration for starting this support group.

International DiGeorge / VCF Support Network Genetic and ...

    https://rarediseases.info.nih.gov/organizations/581
    International DiGeorge / VCF Support Network . c/o Family Voices of New York 46 1/2 Clinton Avenue Cortland, NY 13045 ... Synonyms: Chromosome 22q11.2 deletion syndrome, Velocardiofacial syndrome, VCFS, DiGeorge syndrome, Shprintzen syndrome, Sedlackova syndrome, CATCH22, Autosomal dominant Opitz G/BBB syndrome, Conotruncal anomaly face ...

Pediatric DiGeorge Syndrome (DGS)

    https://www.childrens.com/specialties-services/conditions/digeorge
    Most cases of DiGeorge syndrome are due to a deletion of a group of genes localized to chromosome 22. About 90 percent of patients with DGS have a small deletion in one copy of chromosome number 22. This segment includes an estimated 30 to 40 genes.

Velocardiofacial syndrome (VCFS) resources and support ...

    https://www.chw.org/medical-care/genetics-and-genomics-program/programs-and-services/velocardiofacial-syndrome-vcfs-program/vcfs-resources-and-support
    VCFS Parent Support Network . The VCFS Parent Support Network is a Greater Wisconsin group for families living with Velocardiofacial Syndrome (VCFS) or 22Q Deletion Syndrome. Our support network offers: Networking for children and their parents ; Professionals knowledgeable on subjects concerning school, health, etc. Family get-togethers

Growth Charts - 22q.org

    http://www.22q.org/resources-for-22q/growth-charts-2/
    Growth Charts for 22q11 Deletion Syndrome. Growth Hormone Deficiency in Patients With a 22q11.2 Deletion: Expanding the Phenotype . Sources: Alex Habel, 2. Michael-John McGinn II, 2. Elaine H. Zackai, 3. Nancy Unanue and 2. Donna M. McDonald-McGinn; North Thames Cleft Unit, Great Ormond Street Hospital for Children, London, UK; 2.

For Patients and Families The 22q-VCFS Center

    https://www.cincinnatichildrens.org/service/t/22q-vcfs/families
    The 22Q-VCFS Center at Cincinnati Children’s suggests these resources for families seeking information or support. The Tri-State 22Q-VCFS Family Support Network A family support network providing education, support and social activities for individuals and families affected by 22Q-VCFS.

Practical guidelines for managing adults with 22q11.2 ...

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526275/
    22q11.2 Deletion syndrome (22q11.2DS) is the most common microdeletion syndrome in humans, estimated to affect up to 1 in 2,000 live births. Major features of this multisystem condition include congenital anomalies, developmental delay, and an array of early- and later-onset medical and psychiatric disorders.Cited by: 129

DiGeorge syndrome causes, symptoms, diagnosis, prognosis ...

    https://healthjade.net/digeorge-syndrome/
    DiGeorge syndrome (22q11.2 deletion syndrome) is present in 1 out of every 1,000 live pregnancies, in 1 in 68 children with congenital heart disease, and in 5 to 8 percent of children born with cleft palate 4). DiGeorge syndrome is often diagnosed soon after birth with a blood test to check for the genetic fault.

DiGeorge syndrome - Wikipedia

    https://en.wikipedia.org/wiki/DiGeorge_syndrome
    An example of this type of system is the 22q Deletion Clinic at SickKids Hospital in Toronto, Canada, which provides children with 22q11 deletion syndrome ongoing support, medical care and information from a team of health care workers. Epidemiology. DiGeorge syndrome is estimated to affect between one in 2000 and one in 4000 live births.Causes: Genetic (typically new mutation)



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