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Milroy's syndrome

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Milroy's disease is a congenital familial primary lymphoedema which results from vertical autosomal inheritance of a single gene. Typically, it presents as asymmetric swelling of the legs.

It is a rare disease accounting for about 2% of primary lymphoedemas. Men and women are equally affected.


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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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