Beckwith-Wiedemann syndrome
MONDO:0007534Beckwith-Wiedemann syndrome (BWS) is a genetic disorder characterized by overgrowth, tumor predisposition and congenital malformations.
Also known as: BWS, Beckwith-Wiedemann syndrome, Wiedemann-Beckwith syndrome, exomphalos-macroglossia-gigantism syndrome, Beckwith-Wiedemann syndrome chromosome region, EMG syndrome, Wiedemann-Beckwith syndrome (WBS), exomphalos macroglossia gigantism syndrome
46 clinical trials for this condition and its sub-types, 6 tagged with Beckwith-Wiedemann syndrome itself.
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Sub-types of Beckwith-Wiedemann syndrome
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Franceschini Vardeu Guala syndrome 0 trials
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New scan spots tiny pancreatic tumors that cause dangerous low blood sugar
Diagnosis Expanded accessThis study offers expanded access to a PET scan using a radioactive tracer called 18F-DOPA to locate small, insulin-producing lesions in the pancreas. It is for patients with congenital hyperinsulinism, Beckwith-Wiedemann syndrome, or insulinoma who have low blood sugar. The goal…
Sponsor: Children's Hospital of Philadelphia • Aim: Diagnosis
Last updated Jun 27, 2026 12:25 UTC
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2000-Patient study aims to uncover hidden metabolic risks in rare genetic disorders
Knowledge-focused Recruiting nowThis observational study will follow 2000 children and adults with imprinting disorders—rare genetic conditions like Silver-Russell and Prader-Willi syndromes. Researchers aim to describe the natural history of these diseases and identify common metabolic profiles, risks for obes…
Sponsor: Institut National de la Santé Et de la Recherche Médicale, France • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:05 UTC