Rare condition
Intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome
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About Intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome
RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the genes involved (RMI2, TOP3A).
Related conditions
Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).