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Wiedemann-Rautenstrauch syndrome

MONDO:0009910

Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism.

Also known as: Wiedemann Rautenstrauch Syndrome, Wiedemann-Rautenstrauch syndrome, neonatal progeroid syndrome, Wiedemann Rautenstrauch syndrome, progeroid syndrome neonatal, progeroid syndrome, neonatal

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

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Broader categories

Disease (618) Metabolic disease (215) Musculoskeletal system disorder (196) Hereditary disease (172) Skin disorder (123) Bone disorder (47) Inborn errors of metabolism (42) Osteogenesis imperfecta (33) Lipodystrophy (26) Syndromic disease (24)
Trials to join now! 38 Not yet recruiting 10 Not yet finished but already full! 8 Completed 16 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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