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1.
AJNR Am J Neuroradiol ; 28(4): 782-9, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17416839

ABSTRACT

BACKGROUND AND PURPOSE: The imaging appearance of chronic, partially recanalized dural sinus thrombosis has been incompletely described. We sought to more fully characterize the imaging findings of this entity on MR imaging, time-of-flight MR venography (TOF-MRV), and elliptic centric-ordered contrast-enhanced MR venography (CE-MRV). MATERIALS AND METHODS: From a data base of patients with cerebral venous thrombosis, 10 patients were identified with imaging and clinical findings consistent with the diagnosis of chronic, partially recanalized, dural sinus thrombosis. All patients had MR imaging of the brain without and with contrast. Nine patients underwent MRV, and 6 had both CE-MRV and TOF-MRV. Thirty-four venous segments were thrombosed and were assessed in detail for multiple imaging features. RESULTS: Most thrombosed segments were isointense to gray matter on T1-weighted images (85%), and hyperintense to gray matter on T2-weighted images (97%). Visible serpiginous intrathrombus flow voids were visible in 23 segments (8/10 patients) corresponding with areas of flow signal intensity on TOF-MRV and enhancing channels on contrast MRV. Eighty-four percent of thrombosed segments enhanced equal to or greater than venographically normal venous sinuses. TOF-MRV and CE-MRV were abnormal in all patients, and CE-MRV more completely characterized the thrombosed segments. The imaging appearance did not change in those patients with follow-up imaging (average 13.6 months). CONCLUSION: Chronic, partially recanalized, venous thrombosis has a characteristic appearance on MR and MRV. CE-MRV was abnormal in all cases, despite the intense enhancement of the thrombosed segments. Because of the highly selected nature of the cases reported, further study is required to determine whether these findings are present in all cases of this condition.


Subject(s)
Contrast Media , Magnetic Resonance Angiography , Magnetic Resonance Imaging , Sinus Thrombosis, Intracranial/pathology , Adult , Aged , Cerebrovascular Circulation , Chronic Disease , Female , Humans , Male , Middle Aged , Sinus Thrombosis, Intracranial/physiopathology
2.
Am J Hum Genet ; 69(6): 1236-44, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11704924

ABSTRACT

Although genomewide scans have identified several potential chromosomal susceptibility regions in several human populations, finding a causative gene for type 2 diabetes has remained elusive. Others have reported a novel gene, calpain-10 (CAPN10), located in a previously identified region on chromosome 2q37.3, as a putative susceptibility gene for type 2 diabetes. Three single-nucleotide polymorphisms (SNPs) (UCSNP43, UCSNP19, and UCSNP63) were shown to be involved in increased risk of the disease among Mexican Americans. We have tested the association of these three SNPs with type 2 diabetes among the Samoans of Polynesia, who have a very high prevalence of the disease. In the U.S. territory of American Samoa, prevalence is 25% and 15% in men and women, respectively, whereas, in the independent nation of Samoa, prevalence is 3% and 5% in men and women, respectively. In our study sample, which consisted of 172 unrelated affected case subjects and 96 control subjects, we failed to detect any association between case subjects and control subjects in allele frequencies, haplotype frequencies, or haplotype combinations of UCSNP43, -19, and -63. Also, our data showed no evidence of linkage, among 201 affected sib pairs, in the region of chromosome 2 that contains these SNPs. Three plausible scenarios could explain these observations. (1) CAPN10 is a susceptibility gene only in particular ethnic groups; (2) our study lacks power to detect the effects of CAPN10 polymorphisms (but our sample size is comparable to that of earlier reports); or (3) the underlying biological mechanism is too complex and requires further research.


Subject(s)
Calpain/genetics , Diabetes Mellitus, Type 2/genetics , Genetic Predisposition to Disease/genetics , Polymorphism, Single Nucleotide/genetics , Adult , Aged , Aged, 80 and over , Chromosome Mapping , Chromosomes, Human, Pair 2/genetics , Diabetes Mellitus, Type 2/epidemiology , Ethnicity/genetics , Female , Gene Frequency/genetics , Haplotypes/genetics , Humans , Linkage Disequilibrium/genetics , Lod Score , Male , Middle Aged , Prevalence , Samoa/epidemiology , Sample Size
3.
Br J Oral Surg ; 18(2): 125-31, 1980 Sep.
Article in English | MEDLINE | ID: mdl-6934803

ABSTRACT

An attempt is made to correlate mesio-angular, horizontal, disto-angular and vertical tooth impaction with the incidence, displacement and management of fractures in the region of the mandibular third molar. Evidence was taken principally from a radiographic study of 47 cases of fracture of the mandible at this site. No particular single mandibular third molar angulation showed itself more commonly in this series of fractures. However, fractures involving unerupted mesio-angular third molard tended to remain undisplaced and could, therefore, be treated by simpler measures.


Subject(s)
Mandibular Fractures/complications , Tooth, Impacted/complications , Adolescent , Adult , Female , Humans , Male , Mandibular Fractures/surgery , Middle Aged , Molar , Tooth Eruption
4.
Br J Oral Surg ; 18(2): 175-82, 1980 Sep.
Article in English | MEDLINE | ID: mdl-6934812

ABSTRACT

A case is reported of a metastatic lesion of the mandibular condyle which subsequently confirmed a primary adenocarcinoma in the prostate gland. Attention is drawn to the diffuculties of diagnosis in the absence of a pertinent previous medical history.


Subject(s)
Adenocarcinoma/secondary , Mandibular Neoplasms/secondary , Prostatic Neoplasms/pathology , Adenocarcinoma/pathology , Aged , Humans , Male , Mandibular Condyle/pathology
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