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a loss of function mutation in the SURF1 gene in a 2-year - old girl presenting with failure to thrive , global neurodevelopmental regression , and lactic(passive) caused bysystemic cytochrome oxidase deficiency
Molybdenum deficiencycausessulfite oxidase deficiency
the factorscan causea deficiency in diamine oxidase
mutation in MAT1A gene [ 44(passive) is caused byMethionine adenosyltransferase deficiency
mutations in the MTHFR gene(passive) is caused byMethylene tetrahydrofolate reductase deficiency
a genetic conditionresultingin a Diamine Oxidase deficiency
recessive and dominant mutations(passive) is caused byMethionine adenosyltransferase deficiency
Phenolleadsoxidase deficiency
genetic defectscausingsulfite oxidase deficiency
a set of symptoms(passive) caused bya set of symptoms
histamine intolerancemay causehistamine intolerance
a mitochondrial myopathy(passive) caused bya mitochondrial myopathy
Hypertrophic cardiomyopathy(passive) caused byHypertrophic cardiomyopathy
to muscle weakness ( myopathy ) , poor muscle tone ( hypotonia ) , severe brain dysfunction ( encephalomyopathycan leadto muscle weakness ( myopathy ) , poor muscle tone ( hypotonia ) , severe brain dysfunction ( encephalomyopathy
the rare genetic disorder - Xanthinuriacausesthe rare genetic disorder - Xanthinuria
muscle fibers to become atrophiccausesmuscle fibers to become atrophic
some signal intensity changes in the basal ganglia , with mild white matter atrophy ... but it does not have the severe cystic changes in ISOD ( 9does causesome signal intensity changes in the basal ganglia , with mild white matter atrophy ... but it does not have the severe cystic changes in ISOD ( 9
Weww - known syndromes(passive) caused byWeww - known syndromes