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H415

Glukose-6-fosfatase (G-6-Pase) katalyserer terminaltrinnene i både glukonogenese og glykogenolyse.

10 Arbeidsdager

Spesifikasjoner

Breeds

Gene

Organ

specimen

Svaber, EDTA blod, heparinblod, sæd, vev

Mode of Inheritance

Chromosome

Also known as

Year Published

Generell informasjon

Glukose-6-fosfatase (G-6-Pase) katalyserer terminaltrinnene i både glukonogenese og glykogenolyse. Enzymet er aktivt i høye nivåer i leveren, nyrene, tarmen og bukspyttkjertelen. Mangel på G-6-Pase-enzymet forårsaker glykogenlagringssykdom type Ia (GSD-Ia) (von Gierke sykdom), en autosomal recessiv lidelse.

Kliniske egenskaper

One of the hallmark symptoms of GSD-Ia is recurrent episodes of low blood sugar (hypoglycemia). This is due to the inability of the body to release stored glucose from glycogen when needed, leading to inadequate fuel for the body's energy needs. This accumulation of glycogen can occur in the cells of the liver and kidney causing an enlarged liver (hepatomegaly) or kidney (nehromegaly) and potentially distention of the abdomen. It can also cause delays in growth and development due to the inability to properly metabolize energy.

Other symptoms can include: 1) elevated levels of fats (lipids) in the blood (hyperlipidemia), including cholesterol and triglycerides. 2) buildup of lactic acid in the body can occur due to the impaired metabolic pathways in GSD-Ia. This can lead to fatigue, muscle weakness, and other symptoms. 3) elevated levels of uric acid in the blood can occur in GSD-Ia, leading to an increased risk of gout and kidney stones. 4) during episodes of hypoglycemia, individuals may display symptoms such as weakness, sweating, tremors, confusion, and in severe cases, seizures or loss of consciousness.

Tilleggsinformasjon

Referanser

Pubmed ID: 9259982

Omia ID: 418

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