When PBC is associated with calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasias (CREST) symptoms, it has been proposed to be a distinct clinical entity. Moreover, PBC associated with CREST syndrome has been described in many case reports. However, complete ...
What is scleroderma CREST syndrome? What is the pathophysiology of inflammation? How does pneumonia cause pneumothorax? What is mild chronic obstructive pulmonary disease? What is inherited thrombotic thrombocytopenic purpura? Why does sarcoidosis affect the facial nerve?
We report a 36-year-old female with longstanding oily diarrhea and new-onset dysphagia that was diagnosed as celiac disease and esophagus adenocarcinoma. Celiac is a multisystemic autoimmune disease associated with a longstanding inflammatory process, especially in the gastrointestinal tract. This chronic...
Herein we describe the identification of three isotypes of human ninein by expression library screening with autoimmune sera from CREST patients. All three ninein isotypes exhibit centrosomal localization throughout the cell cycle when GFP-tagged fusion proteins are expressed transiently in mammalian ...
Even if GERD is caused by an autoimmune process as this study suggests, the initial trigger seems to be acid inappropriately moving from the stomach to the esophagus. But that does not mean GERD & NERD are caused by too much stomach acid, as the common dogma holds. ...
Is Jacobsen syndrome autosomal? How common is Guillain-Barre syndrome? How is chronic traumatic encephalopathy diagnosed? How is Asperger syndrome a unique form of ASD? What is scleroderma CREST syndrome? How does Rett syndrome affect communication?
See syndrome, de Morsier. motility test See test, motility. motion after-effect See after-effect, waterfall. See under the nouns. See cortex, motor. motor end-plate See muscle, extraocular. motor field See field of fixation. motor fusion See fusion, motor. See neuron. motor pathway A path...
Certain germinal mutations of MEN1, which encodes MENIN, cause multiple endocrine neoplasia type 1 (ref. 15), which is an autosomal-dominant syndrome characterized by concurrent parathyroid adenomas, gastroenteropancreatic tumours and several other tumour types. Menin does not share significant amino-...
What is scleroderma CREST syndrome? What is the pathogenesis of anemia of chronic disease? What is white matter degenerative disease? What is a moderate degenerative disease in the knee? What is a genetic neurodegenerative disease? What is a degenerative brain disease?
What is autoimmune atrophic gastritis? What causes melanocytic nevi? What is proprioceptive dysfunction? What is Rett syndrome? What is the pathogenesis of Hashimoto's thyroiditis? What is the pathophysiology of anemia? What is cirrhosis of the liver?