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・ Pyrus elaeagrifolia
・ Pyrus hakkiarica
・ Pyrus nivalis
・ Pyrus oxyprion
・ Pyrus pashia
・ Pyrus pyraster
・ Pyrus pyrifolia
・ Pyrus salicifolia
・ Pyrus Series
・ Pyrus serikensis
・ Pyrus syriaca
・ Pyrus ussuriensis
・ Pyrus × bretschneideri
・ Pyrus × sinkiangensis
・ Pyruvate carboxylase
Pyruvate carboxylase deficiency
・ Pyruvate cycling
・ Pyruvate decarboxylase
・ Pyruvate dehydrogenase
・ Pyruvate dehydrogenase (acetyl-transferring)
・ Pyruvate dehydrogenase (cytochrome)
・ Pyruvate dehydrogenase (lipoamide) alpha 1
・ Pyruvate dehydrogenase (lipoamide) alpha 2
・ Pyruvate dehydrogenase (lipoamide) beta
・ Pyruvate dehydrogenase (NADP+)
・ Pyruvate dehydrogenase (quinone)
・ Pyruvate dehydrogenase complex
・ Pyruvate dehydrogenase deficiency
・ Pyruvate dehydrogenase kinase
・ Pyruvate dehydrogenase lipoamide kinase isozyme 1


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Pyruvate carboxylase deficiency : ウィキペディア英語版
Pyruvate carboxylase deficiency

Pyruvate carboxylase deficiency is an inherited disorder that causes lactic acid and other potentially toxic compounds to accumulate in the blood. High levels of these substances can damage the body's organs and tissues, particularly in the nervous system. Pyruvate carboxylase deficiency is a rare condition, with an estimated incidence of 1 in 250,000 births worldwide. This disorder appears to be much more common in some Algonkian Indian tribes in eastern Canada.
==Classification==
Researchers have identified at least three types of pyruvate carboxylase deficiency, which are distinguished by the severity of their signs and symptoms.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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