• Fund Raising and/or Fund Distribution

• 1.

Renu Syndrome United

ReNU Syndrome Variants in RNU42 Uncovered as One of the Most Prevalent Causes of Neurodevelopmental Disorders Discovery Renews Hope for Affected Families Worldwide Characteristics may include Developmental Motor and Intellectual Delays Absent or Delayed Speech and Language Seizures Brain Abnormalities Small Head Size Distinct Facial Features Low Muscle Tone and Drooling Autism Spectrum Disorder Short Stature BoneSkeletal Anomalies Vision Issues and more More Information Big thanks to the researchers clinicians geneticists in these articlesfor this longawaited revelation.

Ring14 USA Outreach Inc

Ring14 Syndrome, Rare disease, Rare epilepsy, nonprofit, support, advocacy, research Ring14 USA is nonprofit 501(c)(3) that supports children and families affected by the rare syndromes of the 14th chromosome, such as Ring14 syndrome.

Cri Du Chat Research Foundation Inc

CDCRF is a 501c3 Non-Profit supporting the development of a treatment for Cri du Chat / 5p- Syndrome.

• Fund Raising and/or Fund Distribution

• 4.

COALITION TO CURE CHD2 INC

Fighting for our kiddos, and others, with CHD2-related neurodevelopmental disorders.

• Birth Defects, Genetic Diseases

• 5.

17q12 Foundation

Creating a community for those affected by 17q12 syndromes while raising awareness and encouraging research.

• Fund Raising and/or Fund Distribution

• 6.

Ava Grace Foundation

For UPD14 Home Ava Gracex27s Story Donate Families Caregivers Medical Professionals Upcoming Events More The Ava Grace Foundation Supporting Families Advancing Research of UPD14Uniparental Disomy of the 14th Chromosome Families Caregivers Information about UPD14 common signs and symptoms getting diagnosed and treatments.

• Birth Defects, Genetic Diseases

• 7.

STXBP1 FOUNDATION

Non-profit dedicated to ending STXBP1-related disorders, rare neurodevelopmental and epileptic encephalopathies, and spreading awareness of this rare disease.

• Single Organization Support

• 8.

THE MED13L FOUNDATION INC

Supporting MED13L families through awareness, research, and community.

• Birth Defects, Genetic Diseases Research

• 9.

THE 11Q RESEARCH AND RESOURCE GROUP INC

home lifesaving protocols who we are frequently asked questions medical support donate More 11qRESEARCH RESOURCE GROUP WELCOMES YOU WHO WE ARE The mission of this website is to provide support and organizational efforts for the parents as well as friends and family of all children with 11th chromosome abnormalities including deletions monosomy duplications trisomy and translocations.