Renata Niemczyk

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In a 50-year-old white woman with stage 3 chronic kidney disease in a course of the autosomal dominant polycystic kidney disease (ADPKD), diagnosed with imaging examination of the abdominal cavity (Fig. 1) and arterial hypertension, Sturge–Weber syndrome (SWS) was diagnosed on the basis of cutaneous [1] and ophthalmologic [2] signs (Fig. 2). Both ADPKD and(More)
Vitreous amyloidosis, a rare condition characteristic of the familial form of systemic amyloidosis with polyneuropathy, is caused by a mutation in the transthyretin (TTR) gene. Herein we have presented 2 sisters with involvement of the vitreous body, which prompted a subsequent diagnosis of the TTR-related, familial form of systemic amyloidosis. Due to the(More)
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