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单词 Lesch-Nyhan syndrome
释义 Lesch-Nyhan syndrome
[`lesh `nī´han ´sin´drōm]
MEDICINE
A hereditary disease of male children, transmitted as an X-linked recessive, characterized by hyperuricemia, deficiency of hypoxanthine-guanine phosphoribosyl transferase, mental retardation, spastic cerebral palsy, choreathetosis, and self-mutilating biting.
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