Cri-du-chat syndrome | ClinicalTrials HQ

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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
Physical Activity and Community EmPOWERment Project	46 XY differences of sex development, Abnormalities, Multiple, Aortic Stenosis, Supravalvular, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Cri-du-chat syndrome, De Lange Syndrome, Down syndrome, Eye Abnormalities, Eye Diseases, Hereditary, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Imprinting Disorders, Male Urogenital Diseases, Musculoskeletal Abnormalities, Neoplasms by Histologic Type, Neoplasms by Site, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Overweight, Pathological Conditions, Signs and Symptoms, Prader-Willi syndrome, Rubinstein-Taybi syndrome, Sex Chromosome Disorders, Signs and Symptoms, Urogenital Abnormalities, Urogenital Diseases, Urogenital Neoplasms, WAGR syndrome, Williams syndrome, Wilms tumor, X-linked disease, aniridia, aortic valve disorder, aortic valve stenosis, autism spectrum disorder, autism, susceptibility to, X-linked 2, benign urinary system neoplasm, bone disorder, cardiovascular disorder, chromosomal disorder, congenital heart disease, disorder of sexual differentiation, dysostosis, endocrine system disorder, eye disorder, fragile X syndrome, gonadal disorder, heart disorder, heart valve disorder, hereditary disease, hereditary neoplastic syndrome, inherited neurodegenerative disorder, intellectual disability, iris disorder, kidney cancer, kidney disorder, mixed neoplasm, musculoskeletal system disorder, neoplasm, nervous system disorder, neurodevelopmental disorder, nutritional disorder, obesity disorder, overnutrition, pervasive developmental disorder, psychiatric disorder, trisomy 13, urinary system disorder, uveal disorder	Recruiting	Not applicable	2026-02-23		NCT06740162