Inherited torticollis
MONDO:0008583A congenital benign lesion that occurs in the distal sternocleidomastoid muscle of infants. It is characterized by the presence of plump spindle cells, and collagenous stroma formation.
Also known as: congenital torticollis, fibromatosis colli, inherited torticollis (disease), torticollis, congenital muscular torticollis, congenital sternomastoid torticollis, congenital wry neck, congenital wryneck
1434 clinical trials for this condition and its sub-types, 3 tagged with Inherited torticollis itself.
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Can a helmet or simple repositioning reshape an Infant's head?
Disease control Recruiting nowThis trial tests two ways to correct flat head syndrome in infants: caregiver-led repositioning and a custom-fit helmet. Researchers will measure head shape changes in treated infants and compare them with a group of typically developing infants. Infants with torticollis will als…
Sponsor: University of Texas Southwestern Medical Center • Aim: Disease control
Last updated Sep 02, 2026 00:00 UTC
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AI aims to cut years off dystonia diagnosis time
Diagnosis Recruiting nowThis study is testing a computer program called DystoniaNet that uses artificial intelligence to help doctors diagnose isolated dystonia, a movement disorder. The trial will enroll 1000 people with dystonia or other conditions that look like it, such as Parkinson's disease or ess…
Sponsor: Massachusetts Eye and Ear Infirmary • Aim: Diagnosis
Last updated Jun 27, 2026 08:01 UTC