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Homocystinuria in Child
Other Resources UpToDate PubMed

Homocystinuria in Child

Contributors: Patricia Ting MD, Ben Barankin MD
Other Resources UpToDate PubMed

Synopsis

Homocystinuria is an autosomal recessive inherited disorder of methionine amino acid metabolism. Homocystinuria encompasses a group of inborn errors of metabolism characterized by elevated serum and urine homocysteine levels. Homocystinuria presents as a multisystem disease involving connective tissue, the cardiovascular / vascular system, and the central nervous system.

Classic homocystinuria is due to mutations in the cystathionine beta-synthase gene on chromosome 21q22.3 resulting in cystathionine beta-synthase enzyme deficiency. Excess homocysteine is remethylated to methionine, which, along with its metabolites, is toxic to the nervous system. Normal life span may occur with early intervention in vitamin B6 (pyridoxine) responders. Otherwise, life expectancy is reduced from thromboembolic complications (approximately 25%-50% by age 30).

Other types of homocystinuria may result from defects in methionine synthase or methionine synthase reductase and defects in vitamin B12 (cyanocobalamin) metabolism. These patients do not present with increased methionine levels on neonatal screens. However, clinical manifestations are similar to those of classic homocystinuria.

Homocystinuria is relatively rare (approximately 1:300 000 worldwide) with a higher incidence in Ireland. It occurs more often in males than females.

Codes

ICD10CM:
E72.11 – Homocystinuria

SNOMEDCT:
11282001 – Homocystinuria

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Last Updated:01/17/2022
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Homocystinuria in Child
A medical illustration showing key findings of Homocystinuria : Seizures, Kyphoscoliosis, Reticular - netlike, Ectopia lentis, Developmental delay, Loss of pigment
Clinical image of Homocystinuria - imageId=231225. Click to open in gallery.  caption: 'Pigmentary dilution of skin and blue eye color.'
Pigmentary dilution of skin and blue eye color.
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