Abstract | BACKGROUND: METHODS: A 31-year-old adult male patient with thrombotic microangiopathy, which was complicated with repeated episodes of acute renal failure, is reported. We suspected that the patient had USS and performed assays of ADAMT13 activity and its inhibitor, followed by ADAMTS13 gene analysis of the patient and his parents. RESULTS: The patient had extremely low ADAMTS13 activity and has no inhibitors of ADAMTS13. Through an ADAMTS13 gene analysis of this family, we found two novel mutations responsible for the disease: a missense mutation in exon 7 [702 C --> A (H234Q)] from the father and a nonsense mutation in exon 26 [3616 C --> T (R1206X)] from the mother. CONCLUSIONS: Our experience appears to indicate the importance of assays of ADAMTS13 activity and its inhibitor in patients who have episodes of renal insufficiency in association with thrombotic microangiopathy, for diagnosis and choice of treatment.
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Authors | Yugo Shibagaki, Masanori Matsumoto, Koichi Kokame, Shigeyoshi Ohba, Toshiyuki Miyata, Yoshihiro Fujimura, Toshiro Fujita |
Journal | Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
(Nephrol Dial Transplant)
Vol. 21
Issue 5
Pg. 1289-92
(May 2006)
ISSN: 0931-0509 [Print] England |
PMID | 16449289
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- ADAM Proteins
- ADAMTS13 Protein
- ADAMTS13 protein, human
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Topics |
- ADAM Proteins
(genetics)
- ADAMTS13 Protein
- Acute Kidney Injury
(diagnosis, genetics, therapy)
- Adult
- Disease Progression
- Follow-Up Studies
- Gene Expression Regulation
- Genetic Carrier Screening
- Genetic Predisposition to Disease
- Hemolytic-Uremic Syndrome
(diagnosis, genetics, therapy)
- Humans
- Male
- Mutation, Missense
- Pedigree
- Purpura, Thrombotic Thrombocytopenic
(diagnosis, genetics, therapy)
- Recurrence
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