A 37-years-old Menkes disease patient - Residual ATP7A activity and early copper administration as key factors in beneficial treatment

Abstract

Menkes disease is a lethal disorder characterized by severe neurological symptoms and connective tissue abnormalities; and results from malfunctioning of cuproenzymes, which cannot receive copper due to a defective intracellular copper transporting protein, ATP7A. Early parenteral copper-histidine supplementation may modify disease progression substantially but beneficial effects of long-term treatment have been recorded in only a few patients. Here we report on the eldest surviving Menkes disease patient (37 years) receiving early-onset and long-term copper treatment. He has few neurological symptoms without connective tissue disturbances; and a missense ATP7A variant, p.(Pro852Leu), which results in impaired protein trafficking while the copper transport function is spared. These findings suggest that some cuproenzymes maintain their function when sufficient copper is provided to the cells; and underline the importance of early initiated copper treatment, efficiency of which is likely to be dependent on the mutant ATP7A function.

Graphical Abstract

Menkes disease is a lethal disorder of copper metabolism, characterized by severe neurological symptoms and connective tissue abnormalities. The eldest surviving Menkes disease patient (TLH) with p.(Pro852Leu) ATP7A variant has been receiving early-onset and long term copper treatment with highly beneficial outcome.

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