proximal 16p11.2 microdeletion syndrome

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight	2q37 microdeletion syndrome, Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cri-du-chat syndrome, Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome, Neurobehavioral Manifestations, Neurologic Manifestations, autism spectrum disorder due to AUTS2 deficiency, central nervous system malformation, chromosomal disorder, chromosome 15q13.3 microdeletion syndrome, chromosome 15q24 deletion syndrome, chromosome 1q21.1 deletion syndrome, chromosome 1q21.1 duplication syndrome, cornea plana 1, autosomal dominant, developmental and epileptic encephalopathy, 4, hereditary disease, hereditary sensory and autonomic neuropathy, inherited neurodegenerative disorder, intellectual disability, intellectual disability, X-linked 1, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, proximal 16p11.2 microdeletion syndrome, rhabdoid tumor predisposition syndrome 2	Recruiting	Not stated	2026-07-23		NCT01238250

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