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Prognostic significance of his to pathological subtypes in stage I pure yolk sac tumour of the ovary. Endodermal sinus tumor and embryonal carcinoma of the ovary in a 53-year-old woman. Secondary leukemia associated with a conventional dose of e to poside: review of serial germ cell tumor pro to cols. Increased risk of myelodysplasia and leukaemia after e to poside, cisplatin, and bleomycin for germ-cell tumours. Review of the granulosa-theca cell tumors from the Emil Novak ovarian tumor registry. Use of monoclonal antibody against human inhibin as a marker for sex cord-stromal tumors of the ovary. Antimullerian hormone as a serum marker of granulosa cell tumors of the ovary: comparative study with serum alpha-inhibin and estradiol. Granulosa cell tumours of the ovary: demographics, survival and the management of advanced disease. Treatment of metastatic stromal tumors of the ovary with cisplatin, doxorubicin, and cyclophosphamide. Clinical parameters and treatment results in recurrent granulosa cell tumor of the ovary. Bleomycin, e to poside, and cisplatin combination therapy of ovarian granulosa cell tumors and other stromal malignancies: a Gynecologic Oncology Group study. Anastrozole therapy in recurrent ovarian adult granulosa cell tumors: a report of 2 cases. Leuprolide acetate for treating refrac to ry or persistent ovarian granulosa cell tumor. Hormonal treatment of a recurrent granulosa cell tumor of the ovary: case report and review of the literature. Gonadotropin-releasing hormone agonist analog therapy effective in ovarian granulosa cell malignancy. Platinum based chemotherapy to treat recurrent Ser to li-Leydig cell ovarian carcinoma during pregnancy. Malignant mixed mesodermal ovarian tumor treatment and prognosis: a 20 year experience. The role of chemotherapy in malignant mixed mullerian tumors of the female genital tract.
Diseases
- Dyscalculia
- Progeria
- Thanatophoric dysplasia cloverleaf skull
- Palmoplantar Keratoderma
- Trypanophobia
- 49, XXXXX syndrome
- Deafness, autosomal dominant nonsyndromic sensorineural
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The cranial deformity is depen early surgical intervention with orthodontic therapy. Prop to sis with strabis tion of supernumerary teeth and overretained primary teeth, mus and orbital hypertelorism is common. Optic nerve when the root formation of succedaneous teeth is greater damage occurs in 80% of cases. Early surgical exposure of ing in narrowing of the maxillary arch and a compressed, unerupted teeth has resulted in stimulation of cementum high-arched palate. Bilateral posterior lingual cross-bites are formation and eruption of the dentition with normal root common. Orthognathic surgery for correction of the riorly positioned maxilla results in an anterior open bite. A large calvarium with hypoplasia of the maxilla, of the cranial deformity depends on the sutures afected, the shallow orbits, and a relatively large mandible is common. Systemic complications include mental retardation, facial dystrophy to hearing loss, speech and visual impair hearing loss, speech and visual impairment, and convulsions. Ultrasonic Etiology and Pathogenesis prenatal diagnosis of exophthalmos has been reported. Craniofacial dysos to sis is inherited in an au to somal-domi Early recognition is essential to guide growth and develop nant mode, with complete penetrance and variable ment of the face and cranium. Failure mental defciency is noted, or intracranial pressure contin of the inferior alveolar artery to develop an ancillary vascu ues to rise. Treatment includes the surgical placement of lar supply gives rise to mandibular abnormalities. Improper artifcial sutures to allow growth of the brain while mini orientation and hypoplasia of the mandibular eleva to r mizing intracranial pressure and secondary calvarial defor muscles, resulting from an aplastic or hypoplastic zygomatic mities. The syndrome seems to be limited to Dysos to sis) defects of the bones and soft tissue of the face. Vascularization Treacher Collins syndrome primarily afects structures of the posterior portion of the second visceral arch by the developing from the frst branchial arch, but it also in stapedial artery seems unimpaired. Indi viduals have a convex facial profle with a prominent nose Clinical Findings and a retrusive chin. It is generally a bilateral anomaly Treacher Collins syndrome is a manifestation of combined with a characteristic facies, including downward sloping developmental anomalies of the second, and mainly, frst of the palpebral fssures, colobomas of the lower eyelid, branchial arches.
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In cases where both sides are 79 presenting expert scientific evidence, assessing the evidence pre-trial allows any areas of agreement to be identified, thus enabling the focus during the trial to be on any issues in dispute (Fraser et al. It is for these reasons that any forensic evidence, well establish or newly emerging must be scrutinised continually for their reliability and their appropriateness for application in criminal proceedings. This should continually be borne in mind for forensic experts across the spectrum of the field, in a bid to strive to always uphold the utmost of excellence in expert evidence with the ultimate goal of avoiding miscarriages of justice. The issues discussed have highlighted the need for emerging forensic techniques to ensure reliability and validity of methods has been tested and scrutinised, which will form the basis for this research. All studies were conducted with the central aim of establishing statistical support for methods used to identify individuals from pho to graphic images. This began by acquiring a large database of images of the dorsum of the hand, for the purposes of conducting subsequent analysis. This database comprises digital images of the dorsal surface of the hand, along with selected additional information for 53 participants. After expressing an interest in participation, individuals were provided with information, a questionnaire and a consent form (Appendix A). The information document outlined what was expected of participants should they choose to commit to the study. This included details of any perceivable risks to facilitate an informed decision regarding willingness and suitability to participate. Individuals were also provided with contact details for the principal investiga to r and primary academic supervisor, should they have any questions or concerns relating to the project. The first cohort was recruited from the staff and postgraduate students within the College of Life Sciences, University of Dundee, by email advertisement (Appendix B). Individuals that expressed further interest were provided with the necessary information. Upon completion of the consent form, participants were allocated an imaging session. A short presentation was given to these students to provide an overview of the project and to invite them to take part in the study. Individuals that expressed an interest were then invited to attend an imaging session where they would be provided with further information.
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Definition: dilated submucosal veins in the lower third of the esophagus, usu ally secondary to portal hypertension ii. Definition: esophageal irritation and inflammation due to reflux of gastric secretions in to the esophagus 11. Definition: metaplasia of the squamous esophageal mucosa to a more protec tive columnar type because of chronic exposure to gastric secretions ii. Risk fac to rs Heavy smoking and alcohol use Achalasia Plummer-Vinson syndrome Tylosis Prior lye ingestion iii. Definition: congenital stenosis of the pylorus due to marked muscular hyper trophy of the pyloric sphincter, resulting in gastric outlet obstruction 11. Presentation Pyloric stenosis is congenital Onset of regurgitation and vomiting in the second week of life hypertrophy of the pylori, Waves of peristalsis are visible on the abdomen which presents with projectile Palpable oval abdominal mass vomiting and a palpable v. Definition: congenital defect in the diaphragm, resulting in herniation of the abdominal organs in to the thoracic cavity 11. Definition: acute inflammation, erosion, and hemorrhage of the gastric muco sa due to a breakdown of the mucosal barrier and acid-induced injury ii. Gross: multiple, small, round; superficial ulcers of the s to mach and duode num 11. Definition: chronic inflammation of the gastric mucosa eventually leading to atrophy (chronic atrophic gastritis) b. Helicobacter pylori gastritis ii, Most common form of chronic gastritis in the United States Ability of H. Helicobacter pylori detection by the [l3q-urea Curved, gram-negative rods breath test and dotazimne Urease producing (CtO) tests. Other methods Risk of infection increases with age of detection include biopsy Associated with chronic gastritis (type B) (his to logic identification is the Associated with duodenal and gastric peptic ulcers gold standard) and serology. Definition: ulcers of the distal s to mach and proximal duodenum caused by gas tric secretions (hydrochloric acid and pepsin) and impaired mucosal defenses 11. Complications Hemorrhage Iron deficiency anemia Penetration in to adjacent organs Perforation (x-ray shows free air under the diaphragm) Pyloric obstruction b. Location: anterior wall of the proximal duodenum rv, Classic presentation: burning epigastric pain 1-3 hours after eating, which is relieved by food c. Risk fac to rs Dietary fac to rs Smoked fish and meats Pickled vegetables Nitrosamines Benzpyrene Decreased intake of fruits and vegetables H. Presentation Often (90%) asymp to matic until late in the course Weight loss and anorexia Epigastric abdominal pain mimicking a peptic ulcer Early satiety Occult bleeding and iron deficiency anemia iv. Diffuse type Diffuse infiltration of s to mach by poorly differentiated tumor cells Signet-ring cells: nucleus is displaced to the periphery by intracellular mucin Linitis plastica: thickened "leather bottle" -like s to mach viii.
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