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1.
Can J Gastroenterol ; 14 Suppl B: 36B-40B, 2000.
Article in English | MEDLINE | ID: mdl-10938503

ABSTRACT

Hepatitis D (delta) virus (HDV) is an infectious agent that propagates in hepatocytes only in the presence of hepatitis B virus, causing fulminant or chronic hepatitis with liver cirrhosis. HDV is a 36 nm particle that includes a circular RNA genome of 1.7 kilobases with an extensive internal complementary that allows it to fold into a rod-like structure. The relationships among genotypes, sequence variability, geographical distribution and disease severity of HDV remain unknown. Consequently, in the present study, the complete nucleotide sequence of an HDV isolated from a Canadian patient was determined. The viral RNA from serum was amplified using reverse transcription coupled to polymerase chain reaction amplification. The resulting complementary DNA was cloned and sequenced. Sequence analysis revealed that this new isolate contained 1672 nucleotides corresponding to genotype 1, which has a worldwide distribution. Sequencing of four independent clones revealed 17 substitutions, corresponding to an overall sequence variability of 1%. Surprisingly, seven mutations were found in the 48-nucleotide region located between the two highly conserved self-catalytic motifs. This is the first demonstration that many substitutions are identified in this region of HDV, and prompts the present authors to define it as a hypervariable region.


Subject(s)
Hepatitis D/virology , Hepatitis Delta Virus/genetics , Base Sequence , Canada , Genotype , Hepatitis Delta Virus/isolation & purification , Humans , Molecular Sequence Data , RNA, Viral/isolation & purification , Reverse Transcriptase Polymerase Chain Reaction , Sequence Analysis, DNA
2.
J Clin Gastroenterol ; 15(3): 199-204, 1992 Oct.
Article in English | MEDLINE | ID: mdl-1479162

ABSTRACT

Of 213 patients with proctitis of all etiologies seen between 1977 and 1987, we studied an original cohort of 96 patients with idiopathic ulcerative proctitis (mean follow-up of 62 months). The diagnosis was made according to strict inclusion criteria, and all cases with any initial feature suggestive of Crohn's disease were excluded. Follow-up showed that 13 patients (13.6%) eventually progressed to Crohn's disease, usually within the first 3 years of the initial diagnosis of idiopathic ulcerative proctitis. Their clinical, endoscopic and histological features at initial presentation were indistinguishable from those in whom the diagnosis remained that of idiopathic ulcerative proctitis. In nine of 13 of these patients (70.0%), the clinical course was characterized by a more protracted course and a poorer response to standard treatment. Such features were not found in those in whom the diagnosis of idiopathic ulcerative proctitis was maintained. Clinicians should be aware that Crohn's disease may present initially as apparent idiopathic ulcerative proctitis.


Subject(s)
Colitis, Ulcerative/etiology , Crohn Disease/complications , Proctitis/etiology , Adolescent , Adult , Colitis, Ulcerative/diagnosis , Crohn Disease/diagnosis , Female , Follow-Up Studies , Humans , Male , Middle Aged , Proctitis/diagnosis
4.
Dig Dis Sci ; 29(2): 178-82, 1984 Feb.
Article in English | MEDLINE | ID: mdl-6321116

ABSTRACT

A female patient with Peutz-Jeghers syndrome successively developed bilateral breast carcinoma and malignant transformation of a duodenal hamartomatous polyp, from which she died.


Subject(s)
Breast Neoplasms/pathology , Carcinoma, Intraductal, Noninfiltrating/pathology , Duodenal Neoplasms/pathology , Neoplasms, Multiple Primary/pathology , Peutz-Jeghers Syndrome/pathology , Adult , Female , Hamartoma/pathology , Humans , Lymphatic Metastasis , Male , Peutz-Jeghers Syndrome/genetics
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