- very long-chain-acyl-CoA-dehydrogenase (
VLCAD)
results in a
deficiency or
malfunction of the
produced VLCAD enzyme. This
mutation occurs on chromosome...
-
deficiency (
VLCAD deficiency) is a
genetic disorder that
affects the body's
ability to
break down
certain fats. In the β-oxidation cycle,
VLCAD's role involves...
- Very long-chain
specific acyl-CoA dehydrogenase,
mitochondrial (
VLCAD) is an
enzyme that in
humans is
encoded by the
ACADVL gene.
Mutations in the ACADVL...
-
Vitiligo Vitreoretinal degeneration Vitreoretinochoroidopathy dominant VKH
VLCAD deficiency Vocal cord
dysfunction familial Von
Gierke disease Von Hippel–Lindau...
- deficiency,
deficiency of
subtypes of acyl CoA
dehydrogenase (LCAD, SCAD, MCAD,
VLCAD, 3-hydroxyacyl-coenzyme A
dehydrogenase deficiency),
thiolase deficiency...
- nine
classes are
involved in
fatty acid β-oxidation (SCAD, MCAD, LCAD,
VLCAD, and VLCAD2), and the
other four are
involved in
branched chain amino acid...
-
disorders are: Very long-chain acyl-coenzyme A
dehydrogenase deficiency (
VLCAD) - Very long-chain acyl-coenzyme A
dehydrogenase Long-chain 3-hydroxyacyl-coenzyme...
- (HMG deficiency) Very long-chain acyl-coenzyme A
dehydrogenase deficiency (
VLCAD deficiency) Long-chain 3-hydroxyacyl-coenzyme A
dehydrogenase deficiency...
- (MCAD) > 1 in 25,000 Very-long-chain acyl-CoA
dehydrogenase deficiency (
VLCAD) > 1 in 75,000
Trifunctional protein deficiency (TFP) < 1 in 100,000 Carnitine...
- "Tissue-specific
strategies of the very-long
chain acyl-CoA dehydrogenase-deficient (
VLCAD-/-)
mouse to
compensate a
defective fatty acid β-oxidation". PLOS ONE. 7...
