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Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome

MONDO:0014689

Also known as: Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome, KFS4, Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism, Klippel-Feil syndrome 4, autosomal recessive, with nemaline myopathy and facial dysmorphism

37 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Muscle tissue disorder (53) Human disease (14) Klippel-Feil syndrome (11) Myopathy (11) Congenital myopathy (8) Skeletal muscle disorder (8) Disease of genetic or genomic mechanism (2)
Trials to join now! 18 Not yet recruiting 7 Not yet finished but already full! 4 Completed 7 Terminated 1
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  • Scientists gather leftover surgical tissue to unlock secrets of bone disease

    Knowledge-focused Terminated

    This study collected bone, cartilage, skin, and fat tissue from 50 patients undergoing surgery at Children's National Medical Center. The goal was to grow cells from these tissues in the lab and analyze them to better understand bone and connective tissue diseases. The study was …

    Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

    Last updated Jun 27, 2026 07:52 UTC

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