2, 5, 20 Here we describe an Arab-Iranian family in which several

individuals developed cirrhosis of unknown etiology. Homozygosity mapping was used to identify homozygous regions of genomic DNA that were shared by two affected cousins but not by an unaffected family member. The two affected individuals in the family who were available for sampling were homozygous for an inactivating mutation in HSD3B7. The family is remarkable for the variability in age of onset and clinical severity of the disease among affected members. ALT, alanine aminotransferase; ALKP, alkaline phosphatase; AST, aspartate aminotransferase; CT, computerized tomography; FAB-MS, fast atom bombardment ionization mass spectrometry; GGT, gamma glutamyl transferase; SNP, single nucleotide polymorphism. LY2606368 molecular weight The study protocol was approved by the University of Texas Southwestern Institutional Review Board. Fasting blood samples were collected after written informed consent was obtained. Plasma and serum were isolated, aliquoted, and stored at −80°C. Fasting serum levels of glucose, lipids/lipoproteins, and liver enzymes were

measured using an automated analyzer and genomic DNA was extracted from blood using an AutopureLS DNA Extractor (Qiagen, Germantown, MD). To detect candidate genomic regions of extended homozygosity, DNA from the proband (III.14), an affected first cousin (III.5), and an unaffected first cousin (III.6) was very assayed for 2.4 million single nucleotide polymorphisms (SNPs) using the HumanOmni 2.5BeadChip microarray (Illumina, San Diego, CA). Briefly, genomic DNA was denatured and amplified Idasanutlin datasheet overnight at 37°C. The amplified DNA was enzymatically fragmented and then incubated overnight at 48°C with the BeadChip containing locus-specific 50-mer

probes. The array was then washed and a single-base extension reaction was performed using labeled nucleotides to extend the captured DNA template. The BeadChip was imaged using the iScan system and visualized using GenomeStudio software (v. 2010.2). The genotypes from the microarrays were exported from GenomeStudio and analyzed using Partek Genomics Suite software (Partek, St. Louis, MO). All samples were successfully genotyped for >99.4% of all SNPs. Genotypes were analyzed using a Hidden Markov Model to identify extended regions of homozygosity. Homozygosity was compared between the samples using custom Perl scripts. The nine exons of HSD3B7 were amplified by polymerase chain reaction (PCR) from genomic DNA of the proband using flanking oligonucleotides exactly as described.3 Negative ion FAB-MS was used to analyze the bile acids in the serum (0.5 mL) exactly as previously described.21 A 24-year-old Arab woman (III.14) from the southwestern region of Iran (Khuzestan) presented with cirrhosis of unknown etiology complicated by portal hypertension, varices, ascites, and hypersplenism.