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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

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

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Broader categories

Disease (680) Metabolic disease (233) Musculoskeletal system disorder (207) Hereditary disease (176) Skin disorder (132) Bone disorder (51) Inborn errors of metabolism (45) Osteogenesis imperfecta (34) Lipodystrophy (27) Syndromic disease (25)
Trials to join now! 2 Completed 1
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  • Rare fat disorder gene hunt: just 2 patients could unlock answers

    Knowledge-focused Completed

    This study looked for a new gene that causes hereditary lipodystrophy, a rare disease where people lose body fat and often develop diabetes and heart problems. Researchers studied DNA and cells from 2 patients who had the disease but no known genetic cause. The goal was to find t…

    Phase: NA • Sponsor: University Hospital, Bordeaux • Aim: Knowledge-focused

    Last updated Jun 27, 2026 13:00 UTC

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