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Fig. 1 | BMC Nephrology

Fig. 1

From: Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease – a case report

Fig. 1

Segregation of the disease in a family. The black-filled individuals, suffering from ADPKD, are marked with a blue arrow (the carriers of PKD2 mutation), and a red arrow (the carrier of PKD1 mutation). The dead woman with a dashed red arrow is the expected carrier of PKD1 mutation. The green arrow indicates the two members of the family with moderately lowered mental abilities. The proband is marked with a black arrow

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BMC Nephrology

ISSN: 1471-2369

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