Homocystinuria is an inherited disorder in which the body is unable to process certain building blocks of proteins (amino acids) properly. There are ...
Homocystinuria is an inherited disorder that keeps the body from processing the essential amino acid methionine. Amino acids are the building blocks of protein.
Homocystinuria is a disorder of methionine metabolism, leading to an abnormal accumulation of homocysteine and its metabolites (homocystine, homocysteine ...
Classical homocystinuria, also known as cystathionine beta synthase deficiency or CBS deficiency,  is an inherited disorder of the metabolism of the amino acid ...
Homocystinuria information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Homocystinuria is an inherited disorder that affects the metabolism of the amino acid methionine.
A principal feature of uncontrolled homocystinuria is subluxation of the crystalline lens; this is bilateral and approximately symmetrical, and can progress to a ...
Homocystinuria is a rare inherited disease that causes a deficiency of one of several enzymes needed for the breakdown of food ( metabolism ). This enzyme ...
Homocystinuria is inherited in families as an autosomal recessive trait. This means that the child must inherit the non-working gene from both parents to ...
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