vlcad deficiency | Very long-chain acyl-CoA dehydrogenase deficiency -

Keyword	CPC	PCC	Volume	Score	Length of keyword
vlcad deficiency	0.85	1	9049	26	16
vlcad	0.43	1	7849	77	5
deficiency	1.71	0.5	2850	95	10

Keyword	CPC	PCC	Volume	Score
vlcad deficiency	0.56	0.4	6562	96
vlcad deficiency symptoms	1.63	0.7	7746	11
vlcad deficiency genereviews	1.72	0.4	7729	47
vlcad deficiency diet	1.18	0.6	1647	98
vlcad deficiency treatment	1.71	0.2	5510	4
vlcad deficiency icd 10	1.05	0.3	9358	68
vlcad deficiency newborn	1.77	0.1	4978	78
vlcad deficiency prognosis	1.51	0.1	5975	67
vlcad deficiency in infants	1.34	0.7	2843	69
what is vlcad deficiency	1.29	0.3	9862	59

Search Results related to vlcad deficiency on Search Engine

Very long-chain acyl-CoA dehydrogenase deficiency - MedlinePlus
medlineplus.gov

https://medlineplus.gov/genetics/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency/

WebVery long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a condition that prevents the body from converting certain fats to energy, particularly during periods without food (fasting). Explore symptoms, inheritance, genetics of this condition.

DA: 40 PA: 68 MOZ Rank: 56

Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK6816/

WebMay 28, 2009 · Clinical Description. Depending on the severity of very long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency, individuals can present with hypoketotic hypoglycemia, hepatomegaly, cardiomyopathy, and myopathy with recurrent rhabdomyolysis, triggered by a catabolic state.

DA: 29 PA: 7 MOZ Rank: 22

Very long-chain acyl-CoA dehydrogenase deficiency
hrsa.gov

https://newbornscreening.hrsa.gov/conditions/very-long-chain-acyl-coa-dehydrogenase-deficiency

WebSigns of VLCAD deficiency can vary widely and may appear anytime from a few months of age to adulthood. Common illnesses, like a cold or flu, or a long time without food can trigger symptoms. Signs of the condition may include the following: Weakness; Tiredness or lack of energy (lethargy) Enlarged liver (hepatomegaly)

DA: 93 PA: 3 MOZ Rank: 9

Very long chain acyl-CoA dehydrogenase deficiency
nih.gov

https://rarediseases.info.nih.gov/diseases/5508/very-long-chain-acyl-coa-dehydrogenase-deficiency/

WebSummary. Very long chain acyl-CoA dehydrogenase deficiency (VLCAD deficiency) is a condition in which the body is unable to properly breakdown certain fats (called very long-chain fatty acids) into energy, particularly during periods without food (fasting). Signs and symptoms may include low blood sugar (hypoglycemia), lack of …

DA: 28 PA: 75 MOZ Rank: 60

Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD)
rarediseases.org

https://rarediseases.org/rare-diseases/very-long-chain-acyl-coa-dehydrogenase-deficiency-lcad/

WebMar 14, 2024 · Disease Overview. Very long-chain acyl-CoA dehydrogenase deficiency (VLCADD) is a rare genetic disorder of fatty acid metabolism that is inherited in an autosomal recessive pattern. It occurs when an enzyme needed to break down long-chain fatty acids is missing or not working properly.

DA: 92 PA: 49 MOZ Rank: 56

Very long-chain acyl-coenzyme A dehydrogenase deficiency
wikipedia.org

https://en.wikipedia.org/wiki/Very_long-chain_acyl-coenzyme_A_dehydrogenase_deficiency

WebVLCAD (very long-chain-acyl-dehydrogenase) deficiency is exclusively linked to genetic mutations in DNA. A change of the gene that codes for very long-chain-acyl-CoA-dehydrogenase (VLCAD) results in a deficiency or malfunction of the produced VLCAD enzyme. This mutation occurs on chromosome 17 and can be altered via a variety of …

DA: 21 PA: 37 MOZ Rank: 76

Very long-chain acyl-CoA dehydrogenase deficiency
medlineplus.gov

https://medlineplus.gov/download/genetics/condition/very-long-chain-acyl-coa-dehydrogenase-deficiency.pdf

WebVery long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a condition that prevents the body from converting certain fats into energy, particularly during periods without food (fasting). There are three forms of VLCAD deficiency, and they are defined by when the signs and symptoms of the condition begin.

DA: 4 PA: 52 MOZ Rank: 25

Management and diagnosis of mitochondrial fatty acid oxidation …
nature.com

https://www.nature.com/articles/s10038-018-0527-7

WebNov 6, 2018 · VLCAD deficiency is generally classified into three phenotypes based on onset time, but the classification should be comprehensively determined based on genotype, residual enzyme activity, and...

DA: 34 PA: 93 MOZ Rank: 43

Orphanet: Very long chain acyl-CoA dehydrogenase deficiency
orpha.net

https://www.orpha.net/en/disease/detail/26793

WebVery long-chain acyl-CoA dehydrogenase (VLCAD) deficiency (VLCADD) is an inherited disorder of mitochondrial long-chain fatty acid oxidation with a variable presentation including: cardiomyopathy, hypoketotic hypoglycemia, liver disease, exercise intolerance and rhabdomyolysis. ORPHA:26793. Classification level: Disorder. Synonym (s):

DA: 85 PA: 38 MOZ Rank: 34

Adult-onset Very Long-Chain Acyl-CoA Dehydrogenase Deficiency …
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006598/

WebVery long-chain acyl-CoA dehydrogenase deficiency (VLCADD) is a hereditary disorder of mitochondrial long-chain fatty acid oxidation that manifests with variable presentations, including exercise intolerance, cardiomyopathy, and liver disease. Herein, we describe the clinical and genetic manifestations of six patients with adult-onset VLCADD.

DA: 50 PA: 77 MOZ Rank: 15