paraganglioma वाक्य
उदाहरण वाक्य
मोबाइल
- Germline mutations in " SDHD " were first linked to hereditary paraganglioma in 2000.
- Mutations in this gene are associated with paraganglioma . [ provided by RefSeq, Jul 2010 ].
- Germline mutations in the gene can cause familial paraganglioma ( in old nomenclature, Paraganglioma Type PGL4 ).
- Germline mutations in the gene can cause familial paraganglioma ( in old nomenclature, Paraganglioma Type PGL4 ).
- Neoplasms of glomus cells are known as paraganglioma, among other names, they are generally non-malignant.
- By histochemistry, the paraganglioma cells are argyrophilic, periodic acid Schiff negative, mucicarmine negative, and argentaffin negative.
- More than 30 mutations in the SDHC gene have been found to increase the risk of hereditary paraganglioma-pheochromocytoma type 3.
- After an extended illness Sherman died of paraganglioma, a rare neuroendocrine neoplasm, at the Motion Picture & Television Country House and Hospital.
- PGL-1 is associated with SDHD mutation, and most PGL-1 individuals with paraganglioma have affected fathers rather than affected mothers.
- Those with Carney-Stratakis syndrome present with a noncancerous tumor associated with the nervous system called a paraganglioma or pheochromocytoma ( a type of paraganglioma ).
- Those with Carney-Stratakis syndrome present with a noncancerous tumor associated with the nervous system called a paraganglioma or pheochromocytoma ( a type of paraganglioma ).
- The net result is that paranglionic tissue that would normally die after birth remains, and this tissue may be able to trigger paraganglioma / pheochromocytoma later.
- Hemangioblastoma and paraganglioma are less usual intramedullary tumors, but since they are more frequently encountered than ganglioglioma, they should also be included in the differential diagnosis.
- In December 1985, prior to the duo's success in Europe, Mel was treated for malignant paraganglioma, a form of cancer, on her liver.
- Rapid and uncontrolled cell division, along with the formation of new blood vessels, can lead to the development of tumors in people with hereditary paraganglioma-pheochromocytoma.
- An inherited SDHC gene mutation predisposes an individual to the condition, and a somatic mutation that deletes the normal copy of the SDHC gene is needed to cause hereditary paraganglioma-pheochromocytoma type 3.
- People living at higher altitudes ( for example, the Andes mountains ) are known to have an increased rate of benign paraganglioma, with the rate of disease increasing with the altitude of the population.
- "' Carney triad "'( CT ) is characterized by the coexistence of three types of neoplasms, mainly in young women, including gastric gastrointestinal stromal tumor, pulmonary chondroma, and extra-adrenal paraganglioma.
- Primary adenocarcinoma of the seminal vesicles, although rare, constitutes the most common neoplasm of the seminal vesicles; even rarer neoplasms include sarcoma, squamous cell carcinoma, yolk sac tumor, neuroendocrine carcinoma, paraganglioma, epithelial stromal tumors and lymphoma.
- A "'paraganglioma "'is a rare metastases . " Paraganglioma " is now the most-widely accepted term for these lesions, that have been also described as : glomus tumor, chemodectoma, perithelioma, fibroangioma, and sympathetic nevi.
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