wordpress-seo domain was triggered too early. This is usually an indicator for some code in the plugin or theme running too early. Translations should be loaded at the init action or later. Please see Debugging in WordPress for more information. (This message was added in version 6.7.0.) in /home/u445773645/domains/acmcasereport.org/public_html/wp-includes/functions.php on line 61141.1. Background: This article aims to provide a comprehensive review of the clinical features and genetics basis of multi-system pseudohypoaldosteronism type 1 caused by SCNN1B gene mutations.
1.1. Introduction: Persistent thorasic airleak is a rare complication after totally implantable port-chamber catheter(PCC) implantation. Prolonged airleaks are undesirable because they prolong the duration of chest tube drainage with associated pain and risk of infection and they also prolong hospitalization. In cancer patients, it is important to prevent this rare complication and to recognize it early if it does occur.
Fibroadenomas (FA), are common benign tumor of the breast, can be treated with simple excision. Breast cancer arising within FA is a rare phenomenon.
To describe the clinical evolution of a case of Epstein-Barr virus infection simulating polymyositis from initial visit to final death
Cardiac amyloidosis is a progressive cardiomyopathy that results from the accumulation of disrupted endogenous proteins in the heart in the form of amyloid fibrils. Diagnosing cardiac amyloidosis is a difficult process for clinicians and requires suspicion first. AL type cardiac amyloidosis is the most fatal type compared to other types of cardiac amyloidosis.
1.1. Introduction: Severe hyperbilirubinemia can cause neurotoxicity called kernicterus which is a neurological syndrome resulting from the deposition of unconjugated bilirubin in the basal ganglia and brainstem nuclei due to which patients suffer from long term morbidities consisting of developmental delays, sensorineural hearing loss, mental retardation and other significant brain damage [1].
1.1. Aims: Over the last decade, molecular methods, such as chromosomal microarray and Bacs-On-Beads assay, have been shown to improve the detection rate of chromosomal abnormalities. Nonetheless, conventional cytogenetics methods, such as FISH and karyotyping, are still useful tools and should not be dismissed.
Juvenile idiopathic arthritis (JIA) is the most common chronic inflammatory arthritis under 16 years of age but unlike rheumatoid arthritis, the risk of cardiovascular diseases including Myocardial Infarction (MI) in adulthood with JIA is not yet proven. This young lady with a background of JIA that progressed to adulthood was diagnosed with inferior wall MI despite no known cardiovascular risk factors. The patient was diagnosed well in time and was successfully thrombolysed with streptokinase
1.1. Objective: Objective to explore the efficacy and safety of IMRT combined with cetuximab in the treatment of locally recurrent nasopharyngeal carcinoma.
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