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Figure 2 | BMC Nephrology

Figure 2

From: Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case report

Figure 2

Pedigree of the index patient with genetic haplotypes and plasma activity of ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type I domain 13). Squares represent males and circles represent females. Plasma ADAMTS13 activity (%) is shown under the circles and squares. Mutations of the ADAMTS13 gene are shown as one-letter amino acid abbreviations numbered from the initial Met codon. The arrow indicates the index patient. The mother and father of the index patient are both asymptomatic carriers. Abbreviations P: patient, ND: not determined.

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