Wilson disease with situs inversus totalis

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Abstract

Situs inversus is a positional anomaly that rotates the abdominal internal visceria and when it is associated with transposition of the thoracic organs it is called situs inversus totalis. Wilson disease (or hepatolenticular degeneration) is an autosomal recessive hereditary disease of human copper metabolism, which causes hepatic and neuropsychiatric symptoms. We describe a case report of situs inversus totalis with Wilson disease, which is the first case to our knowledge.

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APA

Erdogmus, M., Karahan, S., Basak, M., Bulut, K., Avci, D., & Çetinkaya, A. (2013). Wilson disease with situs inversus totalis. European Journal of General Medicine, 10(2), 123–125. https://doi.org/10.29333/ejgm/82293

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