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[Autonomic dysfunction with nocturnal dyspnea (Gerhardt-syndrome) in a patient with multiple system atrophy].
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RESULTS
This case involves a 56-year-old man with a 3-year case history, starting with vertigo, cerebellar symptoms, followed by inspiratory stridor, especially during the night, and autonomic failure with recurrent syncopes. Magnetic resonance imaging confirmed the diagnosis of olivopontocerebellar
[Deterioration of general condition, decreased functional performance, exertional dyspnea].
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Exertional dyspnea: a primary complaint in unusual cases of progressive muscular atrophy and amyotrophic lateral sclerosis.
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Dyspnea as first sign of autonomic failure in postmortem confirmed multiple system atrophy.
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[Carpal tunnel syndrome, bilatal thenar muscular atrophy, proteinuria, shortness of breath, increase in blood sedimentation rate, hypotension and IgG monoclonal gammopathy: (amyloidosis and plasmacytoma)].
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Successful pregnancies in the presence of spinal muscular atrophy: two case reports.
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We report two cases of successful pregnancy in women with chronic, infantile onset, or type II spinal muscular atrophy, both of whom delivered healthy, unaffected babies. The patients required concurrent management by a physiatrist, pulmonologist, and perinatologist throughout the pregnancy.
Only some patients with bulbar and spinal muscular atrophy may develop cardiac disease.
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UNASSIGNED
According to recent publications, some patients with spinal and bulbar muscular atrophy (BSMA) develop cardiac disease, manifesting as ST-segment abnormalities, Brugada-syndrome, dilative cardiomyopathy, or sudden cardiac death. Here we present neurological and cardiac data of a BSMA
Only some patients with bulbar and spinal muscular atrophy may develop cardiac disease.
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UNASSIGNED
According to recent publications, some patients with spinal and bulbar muscular atrophy (BSMA) develop cardiac disease, manifesting as ST-segment abnormalities, Brugada-syndrome, dilative cardiomyopathy, or sudden cardiac death. Here we present neurological and cardiac data of a BSMA
[An autopsy case of progressive generalized muscle atrophy over 14 years due to post-polio syndrome].
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We report the case of a 72-year-old man who had contracted acute paralytic poliomyelitis in his childhood. Thereafter, he had suffered from paresis involving the left lower limb, with no relapse or progression of the disease. He began noticing slowly progressive muscle weakness and atrophy in the
Diagnosis of structural deterioration in an aortic bioprosthetic valve by multidetector row computed tomography: report of a case.
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A 32-year-old female patient presented with shortness of breath. The patient had received aortic valve replacement with a 25-mm bioprosthetic valve at the age of 22, and had had two babies, postoperatively. Ten years later, echocardiography showed the calcifi ed bioprosthetic valve with a high peak
Structural valve deterioration of porcine bioprosthesis soon after mitral valve repair and replacement.
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An 81-year-old woman, who had undergone mitral valve replacement (MVR) with a porcine bioprosthesis after mitral valve repair, presented with hemolysis 4 years and 6 months after MVR. Transthoracic echocardiography (TTE) revealed trivial mitral regurgitation, which was diagnosed based on the
Medialization laryngoplasty with strap muscle transposition for vocal fold atrophy with or without sulcus vocalis.
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OBJECTIVE
Vocal fold atrophy with or without sulcus vocalis may result in a spindle-shaped glottal incompetence (SGI). Because of varying drawbacks with all existing materials (e.g., Silastic block, Teflon, fat, etc.) used for medialization or augmentation of the atrophic vocal folds, there is a
[Severe breathlessness in a patient presenting with chronic bronchitis].
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BACKGROUND
Dyspnoea is the major symptomatic complaint of patients with chronic obstructive pulmonary disease (COPD). Awareness of an unpleasant respiratory sensation, occurs through a complex system of ventilatory control where, as in pain perception, supra-bulbar structures play a major role. In
Acute shortness of breath due to reoccurrence of an intrapericardial bronchogenic cyst.
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A 71-year-old woman presented with dysphagia and acute shortness of breath. Surgical history included a prior thoracotomy overseas for a bronchogenic mesothelial cyst 19 years before. Computed tomography demonstrated a mass within the posterior mediastinum measuring 69 × 70 × 74 mm. A median
Short burst oxygen treatment for breathlessness in chronic obstructive airways disease.
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Most patients with chronic obstructive lung disease prescribed oxygen at home by their family doctor use it for short periods when they feel breathless. Many patients are normoxic. Nineteen patients with advanced disease and variable hypoxaemia undertook exercise until they indicated severe
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