Subjects.  A detailed personal history

via questionnaires from 80 patients of 37 Czech families was obtained. All patients had laboratory and with two exceptions also clinical findings consistent with a diagnosis of HAE. The clinical phenotype of patients was graded using two scoring systems. The first one, based on the localization and frequency of attacks, was adopted from Cumming et al. [7] JNK inhibitor solubility dmso (score 1). The second one used the former system modified by adding criterion regarding the disease onset, and the disease severity was considered by a more complexed approach (score 2) (see Table 1 for details). Becasue of a lack of correlation among particular disease manifestations, patients were also grouped separately according to the number of oedema episodes per year, the age of first angiooedema episode and the overall disease check details severity (see Table 2). All phenotypic data were related to the period without treatment. The control group of general Czech

population included 104 umbilical cord blood samples obtained from consecutively born newborns of Caucasian origin. This group was supplemented by 255 heathy children for MBL2 genotyping [20]. All persons involved in the study (mothers in case of newborns and one of parents in case of children) provided a written statement of informed consent approved by the Ethics Committee of the Centre for Cardiovascular Surgery and Transplantation Brno. Molecular genetic analyses.  DNA was isolated from peripheral blood leucocytes using routine techniques. The polymorphisms −699g/c and 1098a/g

in the BDKR1, and −58c/t and 181c/t in the BDKR2 genes were detected using PCR with subsequent restriction analyses as described previously [16, 21, 22]. PCR products were visualized under UV light after electrophoresis in 3% agarose gel (NuSieve, FMC) and subsequent ethidium bromide staining. The polymorphism D/I in the Idelalisib clinical trial ACE gene was examined using PCR with forward (5′ GCC CTG CAG GTG TCT GCA TGT 3′) and reverse (5′ GGA TGG CTC TCC CCG CCT TGT CTC 3′) primers. Briefly, 100–500 ng of genomic DNA were combined with 25 μl of reaction mix containing 10 mm Tris (pH 8.4), 50 mm KCl, 0.2 mg/ml bovine serum albumin (BSA), 0.2 mm dNTP, 2.0 mm MgCl2, 1.0 μm of each primer and 1 U of Taq polymerase (MBI Fermentas). The PCR amplification was for thirty cycles at 95 °C for 30 s, 62 °C for 30 s and 72 °C for 90 s, with a terminal elongation at 72 °C for 7 min. PCR products of 312 and 599 bp corresponding to D and I variant, respectively, were visualized under UV light after electrophoresis on a 2% agarose ethidium bromide stained gel. Mannose-binding lectin 2 genotyping was performed using multiplex-PCR with sequence-specific primers, as described elsewhere [20]. Mutations in codons 52, 54 and 57 in the coding region and polymorphisms –550g/c and –221c/g in the promotor region of the MBL2 gene were detected.