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 boys aged 12-17 with hypogonadism for a study of an investigational testosterone replacement injection.
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 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.