GENERAL DATA L.B‚ 59/F right handed‚ Catholic‚ presently residing at Famy Laguna. Admitted for the 1st time at QMMC last January 17‚ 2012. CHIEF COMPLAINT: Abdominal pain radiating to the back HISTORY OF PRESENT ILLNESS: The patient was apparently well until 4 days PTA‚ the patient experience abdominal pain located in the epigastric area described as stabbing pain after tasting oily viand that she cooked. She did not took any medication or seek any consult. 2 days prior to admission
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Mucinous cystic neoplasms (MCN) are a group of rare pancreatic lesions that include benign cystadenomas and malignant cystadenocarcinomas. Middle aged women are almost exclusively affected‚ with a female to male predominance of 20:1 and an average age of diagnosis of 50. Affected individuals are frequently asymptomatic and lesions are discovered incidentally. Few present with nonspecific symptoms‚ such as abdominal pain‚ or sequelae of metastatic spread. Wide-spread availability and improved resolution
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aetermi*‚1 lever crysrauinatr’tar me siricir;d; Dustin highconcentrations may yolllg to eyes.Flushwirh rvatersnd svoid prolonged ‚rr t repeeted contact. conruk a phyrician if irrltedon penisn. Prclonged breathing dustmaycause of cancer‚ pulmonary fibrosis‚ anphlsen:a.
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Gadolinium is a paramagnetic metal icon. These paramagnetic icons move differently within a magnetic field in which these make the gadolinium useful for something more familiar in today’s medicine such as MRI. Gadolinium helped doctors and medical professionals to be able to see a patient’s internal organs‚ inflammation‚ tumors‚ blood vessels‚ and tissue. The quality of MRI’s are enhanced by altering the magnetic properties of water molecules when gadolinium is used. Gadolinium used by itself is
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oxygen‚ eventually requiring intubation with mechanical ventilation in order to maintain his oxygenation. He underwent an open lung biopsy an attempt to delineate the etiology of his pulmonary situation‚ and this was reported as idiopathic pulmonary fibrosis and abilities. The specimen was sent to the Forest General Pathology Department for further evaluation‚ and they were able to give no further help concerning the ideology pf his pulmonary status. An echocardiogram showed left ventricular walls motion
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eventually requiring intubation with mechanical ventilation in order to maintain his oxygenation. He underwent an open-lung biopsy in an attempt to delineate the etiology of his pulmonary situation‚ and this was reported as idiopathic pulmonary fibrosis in alveolitis. The specimen was sent to the mayo clinic pathology department for further evaluation‚ and they were able to give no further help concerning the ideology of his pulmonary status. An echocardiogram showed left ventricular wall motion
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eventually requiring intubation with mechanical ventilation in order to maintain his oxygenation. He underwent an open lung biopsy in an attempt to delineate the etiology of his pulmonary situation‚ and this was reported as idiopathic pulmonary fibrosis and alveolitis. The specimen was sent to the Forest General Pathology department for further evaluation‚ and they were able to give no further help concerning the etiology of his pulmonary status. An echocardiogram showed left ventricular wall
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nutrition into stressful areas of daily life. (Johns Hopkins Cystic Fibrosis Center‚ 2016). Changing those areas can help a person gain a more rewarding lifestyle. For example: completing shopping for the week‚ or planning out a schedule of meals and snacks. By doing this the patient can feel in control of their time; which can create less stress while making better nutritional food choices; as it is planned out (Johns Hopkins Cystic Fibrosis Center‚ 2016). The best way to reduce daily stress is organizing
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Key: Male affected with cystic fibrosis Unaffected male female affected with cystic fibrosis unaffected female Generation I II III IV V Pedigree showing inheritance of cystic fibrosis A Key: Male affected with cystic fibrosis Unaffected male female affected with cystic fibrosis unaffected female Generation I II III IV V Pedigree showing inheritance of cystic fibrosis A Questions: 1. According to the pedigree‚ is cystic fibrosis inherited as a dominant or
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Questions: 1. According to the pedigree‚ is cystic fibrosis inherited as a dominant or as a recessive trait? Explain how you made your conclusion using evidence from the pedigree and the principles of genetics. Cystic Fibrosis is a recessive trait. You have to inherit two copies of the allele to have cystic fibrosis. If you have just one of these alleles you could be a carrier of cystic fibrosis‚ but have absolutely no symptoms. If two carriers of this allele have
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