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Homocystinuria
- Homocystinuria is a genetic disorder that affects the metabolism of the amino acid methionine. Amino acids are ... Homocystinuria is inherited in families as an autosomal recessive trait. This means that the child must inherit ...
- Causes may include: Homocystinuria Marfan syndrome Other rare genetic disorders
- ... disease Cystinosis Cystathioninuria Fructose intolerance Galactosemia Hartnup disease Homocystinuria Hyperammonemia Hyperparathyroidism Maple syrup urine disease Methylmalonic acidemia ...
- ... carinatum (present at birth) Trisomy 18 Trisomy 21 Homocystinuria Marfan syndrome Morquio syndrome Multiple lentigines syndrome Osteogenesis ...