GRACILE syndrome is a severe disorder that begins before birth. GRACILE stands for the condition's characteristic features: growth retardation ...
GRACILE syndrome is an inherited metabolic disease. GRACILE stands for growth retardation, aminoaciduria, cholestasis, iron overload, lactacidosis, and early death.
GRACILE syndrome is a very rare autosomal recessive genetic disorder, one of the Finnish heritage diseases. It is caused by mutation in BCS1L gene that occurs in 1 ...
What is GRACILE Syndrome? GRACILE syndrome is a fatal inherited disorder caused by a mutation in a gene necessary for providing cells with energy.
GRACILE syndrome Synonyms Fellman syndrome, Finnish lactic acidosis with hepatic hemosiderosis, Finnish lethal neonatal metabolic syndrome, Growth Retardation ...
Summary. GRACILE syndrome is an inherited lethal mitochondrial disorder characterized by fetal growth restriction (GR), aminoaciduria (A), cholestasis (C), iron ...
GRACILE syndrome is an inherited disease characterized by poor fetal growth, iron overload, liver damage, and death in infancy.
603358 - gracile syndrome - growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death;; finnish lethal ...
GRACILE syndrome symptoms, causes, diagnosis, and treatment information for GRACILE syndrome (Finnish lethal neonatal metabolic syndrome) with alternative diagnoses ...
1. Am J Hum Genet. 2002 Oct;71(4):863-76. Epub 2002 Sep 5. GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L.