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Congenital Nephrotic Syndrome, Finnish Type

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Congenital Nephrotic Syndrome, Finnish Type

Explore clinical trials studying Congenital Nephrotic Syndrome, Finnish Type. Study availability and eligibility vary by location and protocol.

1 public trial 0 recruiting studies

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Congenital Nephrotic Syndrome, Finnish Type trial results

Completed

Baby Detect : Genomic Newborn Screening

NCT05687474

Conditions: 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
Locations: CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium

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