Pyruvate carboxylase deficiency

（重定向自Pyruvate carboxylase deficiency disease）

Pyruvate carboxylase deficiency has an autosomal
recessive pattern of inheritance.

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.

单词	Pyruvate carboxylase deficiency disease
释义	Pyruvate carboxylase deficiency disease 英语百科 Pyruvate carboxylase deficiency （重定向自Pyruvate carboxylase deficiency disease） 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.
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