Natural History Study For Rare And Ultrarare Neurological Diseases
Seeking people who have a diagnosis of a rare or ultrarare neurological disease.
Seeking people who have a diagnosis of a rare or ultrarare neurological disease.
Seeking infants aged 6-8 months who have an older sibling with autism for a study to determine if intensive early intervention before at 15 months improves communication and language skills at 24 months.
Seeking infants admitted to the NICU with an unexplained likely genomic illness for a study of the benefit of genomic testing on their care.
Seeking teens aged 15-18 years old who were enrolled in the ELGAN study of premature infants between April 2002 and August 2004 for a follow-up study of health and developmental progress.
Seeking boys and girls with Fragile X Syndrome who were born between 2003 and 2017 for a registry to better understand how to manage and treat Fragile X Syndrome.