GRACILE syndrome

GRACILE syndrome is an inherited lethal mitochondrial disorder characterized by fetal growth restriction (GR), aminoaciduria (A), cholestasis (C), iron overload (I), lactacidosis (L), and early death (E).

Also known as: Fellman disease, Growth restriction-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome, gracile syndrome, FLNMS, Fellman syndrome, Finnish lactic acidosis with hepatic hemosiderosis, Finnish lethal neonatal metabolic syndrome, Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death

13 clinical trials for this condition and its sub-types, 0 tagged with GRACILE syndrome itself.