Homocystinuria

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Homocystinuria
Classification and external resources
Homocysteine
ICD-10	E72.1
ICD-9	270.4
OMIM	236200
DiseasesDB	5991
MedlinePlus	001199
eMedicine	derm/708
MeSH	D006712

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.

Presentation

This defect leads to a multisystemic disorder of the connective tissue, muscles, CNS, and cardiovascular system. Homocystinuria represents a group of hereditary metabolic disorders characterized by an accumulation of homocysteine in the serum and an increased excretion of homocysteine in the urine. Infants appear to be normal and early symptoms, if any are present, are vague.

Signs and symptoms

• A family history of homocystinuria
• Flush across the cheeks
• Tall, thin build
• Long limbs
• High-arched feet (pes cavus)
• Knock-knees (genu valgum)
• Pectus excavatum
• Pectus carinatum
• Mental retardation
• Psychiatric disease
• Eye anomalies:
• 90% have ectopia lentis or subluxation of lens
• Myopia (Nearsightedness)
• Glaucoma
• Optic atrophy
• Seizures
• extensive atheroma formation at young age which affects many arteries but not the coronary arteries
• Charlie Chaplin gait
• Intra vascular thrombosis

Mortality/morbidity

The life expectancy of patients with homocystinuria is reduced only if untreated. It is known that before the age of 30, almost one fourth of patients die as a result of thrombotic complications (e.g. heart attack).

Treatment

No specific cure has been discovered for homocystinuria; however, many people are treated using high doses of vitamin B6 (also known as pyridoxine). Slightly less than 50% respond to this treatment and need to intake supplemental vitamin B6 for the rest of their lives. Those who do not respond require a low methionine diet, and most will need treatment with trimethylglycine. A normal dose of folic acid supplement and occasionally adding cysteine to the diet can be helpful.

Betaine, (N,N,N-trimethylglycine) is used to reduce concentrations of homocysteine by promoting the conversion of homocysteine back to methionine. The re-formed methionine is then gradually removed by incorporation into body protein. The methionine that is not converted into protein is converted to S-adenosyl-methionine which goes on to form homocysteine again. Betaine is, therefore, only effective if the quantity of methionine to be removed is small. Hence treatment consists of a diet low in methionine and betaine. In classical homocystinuria (CBS) the plasma methionine usually increases above the normal range of 30 micromole/l and the concentrations should be monitored as potentially toxic levels (more than 400 micromole/l) may be reached.

Recommended diet

Low-protein food is recommended for this disorder, which requires food products low in particular types of amino-acid (e.g. methionine).

See also

• Cystinuria
• Hyperhomocysteinemia

External links

• Homocystinuria Support
• GeneReview/NIH/UW entry on Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency