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Blue disease
Blue ear disease
Blue-ear disease of pigs
Congenital disease
Congenital metabolic disease
Inborn disease
Inborn error of metabolism
Inborn metabolic disease
Inborn metabolic disorder
MSD
Mysterious pig disease
Mysterious swine disease
Mystery pig disease
New pig disease
PRRS
Porcine epidemical abortion
Porcine reproductive and respiratory syndrome
Purple ears disease
Society for the Study of Inborn Errors of Metabolism

Traduction de «inborn disease » (Anglais → Français) :

congenital disease [ inborn disease ]

maladie congénitale [ maladie innée ]


congenital metabolic disease | inborn metabolic disease

maladie métabolique congénitale


inborn metabolic disease

trouble métabolique congénital


An extremely rare inborn error of sterol biosynthesis with manifestations of facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease. Only 4 cases have been reported in

lathostérolose


inborn error of metabolism | inborn metabolic disorder

maladie enzymatique


blue disease | blue ear disease | blue-ear disease of pigs | mysterious pig disease | mysterious swine disease | mystery pig disease | new pig disease | porcine epidemical abortion | porcine reproductive and respiratory syndrome | purple ears disease | MSD [Abbr.] | PRRS [Abbr.]

maladie bleue | maladie de l'oreille bleue | maladie mystérieuse du porc | mystérieuse maladie des porcs | nouvelle maladie des porcs | nouvelle maladie du porc | syndrome affectant la reproduction et la respiration chez les porcs | syndrome dysgénésique et respiratoire du porc | MMP [Abbr.] | SDRP [Abbr.]


Advisory Committee on Inborn Errors of Metabolism in Children

Comité consultatif sur les enzymopathies des enfants


Society for the Study of Inborn Errors of Metabolism

Society for the Study of Inborn Errors of Metabolism


A rare inborn error of metabolism characterized by persistent hypermethioninemia with increased levels of S-adenosylmethionine and S-adenosylhomocysteine which manifests with encephalopathy, severe global developmental delay, mild to severe liver dys

encéphalopathie associée à une hyperméthioninémie par déficit en adénosine kinase


A rare inborn error of metabolism disorder with early-onset acute encephalopathic episodes (frequently triggered by viral infections) associated with lactic acidosis and alpha-ketoglutaric aciduria which typically manifest with variable degrees of at

encéphalopathie de l'enfant par déficit en thiamine pyrophosphokinase




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Date index: 2024-03-31
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