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J Korean Med Sci. 2011 Jul;26(7):951-3. doi: 10.3346/jkms.2011.26.7.951. Epub 2011 Jun 20.

Identification of a novel mutation in the ATP7A gene in a Korean patient with Menkes disease.

Author information

1
Department of Pediatrics, School of Medicine, Konkuk University, Seoul, Korea.

Abstract

Menkes disease is an infantile-onset X-linked recessive neurodegenerative disorder caused by diverse mutations in a copper-transport gene, ATP7A. Affected patients are characterized by progressive hypotonia, seizures, failure to thrive and death in early childhood. Here, we report a case of Menkes disease presented by intractable seizures and infantile spasms. A 3-month-old male infant had visited our pediatric clinic for lethargy, floppy muscle tone, poor oral intake and partial seizures. His hair was kinky, brown colored and fragile. Partial seizures became more frequent, generalized and intractable to antiseizure medications. An EEG showed frequent posteriorly dominant generalized spikes that were consistent with a generalized seizure. From a genetic analysis, a c.2743C>T (p.Gln915X) mutation was detected and diagnosed as Menkes disease. The mutation is a novel one that has not been previously reported as a cause of Menkes disease.

KEYWORDS:

ATP7A Mutation; MNK Gene; Menkes Disease

PMID:
21738351
PMCID:
PMC3124728
DOI:
10.3346/jkms.2011.26.7.951
[Indexed for MEDLINE]
Free PMC Article

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