Homocystinuria overview: Difference between revisions
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==Overview== | ==Overview== | ||
Homocystinuria, also known as cystathionine beta synthase deficiency, is an inherited disorder of the [[metabolism]] of the [[amino acid]][[methionine]], often involving [[cystathionine beta synthase]]. It is an inherited [[autosomal recessive trait]], which means a child needs to inherit the defective gene from both parents to be affected. | Homocystinuria, also known as cystathionine beta synthase deficiency, is an inherited disorder of the [[metabolism]] of the [[amino acid]][[methionine]], often involving [[cystathionine beta synthase]]. It is an inherited [[autosomal recessive trait]], which means a child needs to inherit the defective gene from both parents to be affected. | ||
==References== | |||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 22:27, 16 August 2013
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Homocystinuria Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ayokunle Olubaniyi, M.B,B.S [2]
Overview
Homocystinuria, also known as cystathionine beta synthase deficiency, is an inherited disorder of the metabolism of the amino acidmethionine, often involving cystathionine beta synthase. It is an inherited autosomal recessive trait, which means a child needs to inherit the defective gene from both parents to be affected.