Homocystinuria.. disorder in the metabolism of methionine due to the absence of hepatic enzyme (Sastathaaon Sncaz) causing abnormality in the formation of collagen

Homocystinuria:
It is caused by a disorder in the metabolism of methionine due to the absence of the hepatic enzyme (systathione synthetase), causing an abnormality in the formation of collagen.
Clinical manifestations:
Clinical manifestations appear early in the first year of life.
- Thin yellowish skin and atrophy scars.
- Sparse hair is thin, brittle and brittle due to decreased bondage of the dali sulfide.
- Intravenous clotting leads to blue-colored interlock.
Treatment:
Diet with low intake of methionine. Giving "pyrodoxine and cysteine" may give good results.