Abstract
Hyperhomocysteinemia (HHcy) has been recognized as a risk factor of several chronic disease. It is noteworthy that HHcy prevalence appeared to be rising in recent years. Many patients have good curative effect after treatment, but some HHcy caused by gene mutations remains difficult to treat. Here, we present a case of hyperhomocysteinemia type II with poor effect of conventional treatment. We report it in order to provide a basis for follow-up studies.
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