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IntroductionNephrotic syndrome is a kidney disorder marked by excessive protein loss in the urine, leading to various systemic complications. This condition often results from damage to the glomeruli—the kidney's filtering units—causing proteinuria, low blood protein levels, and fluid retention. Understanding the assessment, diagnosis, and management of nephrotic syndrome is essential for effective treatment and prevention of further kidney damage.AssessmentPatient History: Document...
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Chronic Kidney Disease (CKD) progressively impairs multiple body systems due to the accumulation of uremic toxins, which disrupt cellular functions across various organs.Neurologic symptomsNeurologic symptoms often arise early in CKD, as uremic toxin buildup drives changes in cognitive and motor functions. Patients frequently experience fatigue, headache, confusion, difficulty concentrating, and, in severe cases, seizures. Peripheral neuropathy commonly manifests as burning sensations in the...
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Endocarditis can present various clinical features depending on the causative organism and the patient's underlying health conditions. Initially, the clinical features of infective endocarditis develop gradually, presenting with nonspecific symptoms that can be easily mistaken for other illnesses.General SymptomsEarly symptoms of infective endocarditis are fever, chills, weakness, malaise, fatigue, and weight loss. These symptoms reflect the systemic nature of the infection and the body's...
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Drug toxicity: Idiosyncratic Reactions01:16

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Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
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Positron Emission Tomography Using 64-Copper as a Tracer for the Study of Copper-Related Disorders
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WILSON'S DISEASE (A report of two cases).

M Kanitkar1, S N JOSHi2, N Dutta Roy3

  • 1Graded Specialist Paediatrics, Military Hospital, Jhansi. 284 001.

Medical Journal, Armed Forces India
|August 4, 2017
PubMed
Summary

Wilson's disease presents diverse clinical outcomes, from fatal hepatic failure to manageable neurological symptoms with zinc therapy. Early diagnosis and appropriate treatment are crucial for Wilson's disease patients.

Area of Science:

  • Hepatology
  • Neurology
  • Medical Genetics

Background:

  • Wilson's disease is a rare inherited disorder of copper metabolism.
  • Accumulation of copper in the liver and brain leads to severe organ damage.
Keywords:
Fulminant hepatic failureWilson's diseaseZinc therapy

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  • Clinical presentation varies widely, complicating diagnosis and management.