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Tradução e análise de palavras por inteligência artificial ChatGPT

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etimologia

O que (quem) é myophosphorylase deficiency glycogenosis - definição

HUMAN DISEASE

Glycogen synthase deficiency; GSD type 0; Glycogenosis, type 0

Glycogen storage disease type 0

Glycogen storage disease type 0 is a disease characterized by a deficiency in the glycogen synthase enzyme (GSY). Although glycogen synthase deficiency does not result in storage of extra glycogen in the liver, it is often classified as a glycogen storage disease because it is another defect of glycogen storage and can cause similar problems.

https://en.wikipedia.org/wiki/Glycogen_storage_disease_type_0

Fluorine deficiency

MEDICAL CONDITION

Fluorine Deficiency; Fluoride deficiency

Fluoride or fluorine deficiency is a disorder which may cause increased dental caries (or tooth decay, is the breakdown of dental tissues by the acidic products released by the "bacterial fermentation of dietary carbohydrates.") and possibly osteoporosis (a bone disorder which leads to a decrease in bone mass, and an increase in bone fragility), due to a lack of fluoride in the diet.

https://en.wikipedia.org/wiki/Fluorine_deficiency

Pseudocholinesterase deficiency

MEDICAL CONDITION

Plasma cholinesterase deficiency; Vysya enzyme deficiency

Pseudocholinesterase deficiency is an autosomal recessive inherited blood plasma enzyme abnormality in which the body's production of butyrylcholinesterase (BCHE; pseudocholinesterase aka PCE) is impaired. People who have this abnormality may be sensitive to certain anesthetic drugs, including the muscle relaxants succinylcholine and mivacurium as well as other ester local anesthetics.

https://en.wikipedia.org/wiki/Pseudocholinesterase_deficiency

Wikipédia

Glycogen storage disease type 0

Glycogen storage disease type 0 is a disease characterized by a deficiency in the glycogen synthase enzyme (GSY). Although glycogen synthase deficiency does not result in storage of extra glycogen in the liver, it is often classified as a glycogen storage disease because it is another defect of glycogen storage and can cause similar problems. There are two isoforms (types) of glycogen synthase enzyme; GSY1 in muscle and GSY2 in liver, each with a corresponding form of the disease. Mutations in the liver isoform (GSY2), causes fasting hypoglycemia, high blood ketones, increased free fatty acids and low levels of alanine and lactate. Conversely, feeding in these patients results in hyperglycemia and hyperlactatemia.

https://en.wikipedia.org/wiki/Glycogen storage disease type 0