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A lipid storage disorder (or lipidosis) is any one of a group of inherited metabolic disorders in which harmful amounts of fats or lipids accumulate in some body cells and tissues. [1] People with these disorders either do not produce enough of one of the enzymes needed to metabolize and break down lipids or, they produce enzymes that do not ...
In the study Children of the 90s, 2.5% born in 1991 and 1992 were found by ultrasound at the age of 18 to have non-alcoholic fatty liver disease; five years later transient elastography found over 20% to have the fatty deposits on the liver, indicating non-alcoholic fatty liver disease; half of those were classified as severe. The scans also ...
Hepatic microvascular dysplasia (HMD or MVD) or portal atresia is a disorder where mixing of venous blood and arterial blood in the liver occurs at the microscopic level. It occurs most commonly in certain dog breeds such as the Cairn and Yorkshire terriers although any dog breed may be at risk. [1] [2] [3] This disease may also be found in cats.
In Bristol University's study Children of the 90s, 2.5% of 4,000 people born in 1991 and 1992 were found by ultrasound scanning at the age of 18 to have non-alcoholic fatty liver disease; five years later transient elastography (fibroscan) found over 20% to have the fatty deposits on the liver of steatosis, indicating non-alcoholic fatty liver ...
Liver disease, or hepatic disease, is any of many diseases of the liver. [1] If long-lasting it is termed chronic liver disease . [ 3 ] Although the diseases differ in detail, liver diseases often have features in common.
Histiocytoma is a benign skin tumor that is more frequent in young dogs (<4 years), and often regresses without treatment. [165] Malignant histiocytosis (histiocytic sarcoma) is an aggressive cancer found primarily in certain breeds including the Bernese Mountain Dog, rottweiler, golden retriever and flat coated retriever.
In children, CPSS may present as neonatal cholestasis. These complications are generally induced by long term portosystemic derivations and are more commonly observed in children than in adults. [9] Unexplained neurocognitive dysfunction and other behavioural issues linked to hepatic encephalopathy occur in 17% to 30% of cases. [7]
One-, two-, and three-year survival rates of 60%, 26%, and 14%, respectively [2] Krabbe disease ( KD ) (also known as globoid cell leukodystrophy [ 3 ] or galactosylceramide lipidosis ) is a rare and often fatal lysosomal storage disease that results in progressive damage to the nervous system .