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Early clinical signs and treatment of Menkes disease. | LitMetric

Early clinical signs and treatment of Menkes disease.

Mol Genet Metab Rep

Unit of Regenerative Diseases Research, Division of Research Promotion and Development, Advanced Medical Research Center, Toho University Graduate School of Medicine, Ota-ku, Tokyo 143-8540, Japan.

Published: June 2022

AI Article Synopsis

Article Abstract

Menkes disease (MD) is an X-linked recessive disorder caused by mutations in . Patients with MD exhibit severe neurological and connective tissue disorders due to copper deficiency and typically die before 3 years of age. Early treatment with copper injections during the neonatal period, before the occurrence of neurological symptoms, can alleviate neurological disturbances to some degree. We investigated whether early symptoms can help in the early diagnosis of MD. Abnormal hair growth, prolonged jaundice, and feeding difficulties were observed during the neonatal period in 20 of 69, 16 of 67, and 3 of 18 patients, respectively. Only three patients visited a physician during the neonatal period; MD diagnosis was not made at that point. The mean age at diagnosis was 8.7 months. Seven patients, who were diagnosed in the prenatal stage or soon after birth, as they had a family history of MD, received early treatment. No diagnosis was made based on early symptoms, highlighting the difficulty in diagnosing MD based on symptoms observed during the neonatal period. Patients who received early treatment lived longer than their elderly relatives with MD. Three patients could walk and did not have seizures. Therefore, effective newborn screening for MD should be prioritized.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861833PMC
http://dx.doi.org/10.1016/j.ymgmr.2022.100849DOI Listing

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