Adult Onset
Adult Onset Still’s Disease
... The adult onset Still’s disease is a rare affection characterised by occurrence of fever, arthralgia or arthritis and evanescent cutaneous ...the adult onset Still’s disease is not well ...
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Probing the neural mechanisms of adult onset isolated focal dystonia
... Adult onset isolated focal dystonia (AOIFD) is inherited in an autosomal dominant manner with a reduced penetrance of 12-15%; cervical dystonia (CD) is the most common phenotype in northern ...developing ...
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Myositis, Vasculitis, Hepatic Dysfunction in Adult-Onset Still's Disease
... Adult-onset Still’s disease (AOSD) is a rare systemic inflam- matory disease of unknown etiology. Hepatic dysfunction is common in AOSD, and more than 70% of these patients show elevated liver enzymes [1]. ...
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Adult Onset Still's Disease and Rocky Mountain Spotted Fever
... We found that our patient’s current symptoms were consistent with Yamaguchi criteria for Adult Onset Still’s disease. We checked her ferritin level which came back markedly elevated at 9362 ng/mL. After ...
5
A Novel Mutation in the Adult-Onset Alexander’s Disease GFAP Gene
... of adult-onset (Type II) AxD patients complain of bulbar signs such as dysphagia and dysphonia, and dysar- thria pyramidal signs such as hyperreflexia and ataxia are also common [5, ...
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An increased incidence of Hodgkin's lymphoma in patients with adult-onset sarcoma
... The International Sarcoma Kindred Study (ISKS) is a prospectively collected familial adult-onset sarcoma cohort, which began recruitment in July 2009. Probands were aged at least 15 years when diagnosed ...
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Adult-onset type II citrullinemia: Current insights and therapy
... Abstract: Citrin deficiency is a recessively inherited metabolic disorder with age-dependent clinical manifestations. It causes neonatal intrahepatic cholestasis (NICCD) and adult-onset type II ...
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Age Related Sexual Dimorphism in Temporal Discrimination and in Adult Onset Dystonia Suggests GABAergic Mechanisms
... of onset in phenotypes of adult-onset ...of onset and sex ratio of five adult-onset dystonia phenotypes (listed in Table S1 in Supplementary ...of onset is statistically ...
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Early Onset Schizophrenia: A Comparative study of Clinical Features and Premorbid Function with Adult Onset Group.
... Thirty patients satisfying the DSM IV criteria for Schizophrenia in the age group 13-18 years (Early onset Schizophrenia group) were evaluated. The cases were chosen from consecutive patients attending the ...
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Adult-onset Still's disease: current challenges and future prospects
... Abstract: Adult-onset Still’s disease (AOSD) – a multi-systemic inflammatory condition characterized by high fevers, polyarthritis, an evanescent rash, and pharyngitis – has been a challenging condition to ...
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Islets of hypoglycaemia: a rare case of adult onset nesidioblastosis
... However, in adults, hyperinsulinemic hypoglycemia is usually caused by insulinomas. Other causes like non- insulinoma pancreatogenous hypoglycemia syndrome and factitious hypoglycaemia are usually very rare and other ...
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Treatment of adult-onset Still’s disease: a review
... Adult-onset Still’s disease is a complex disease with a polymorphic clinical presentation. In some cases, AOSD is as simple as a unique flare easily cured by NSAIDs or short-course corticosteroid therapy. ...
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Temporal discrimination: Mechanisms and relevance to adult onset dystonia
... of onset of adult-onset dystonia and sex ratios; there is a male predominance in phenotypes with age of onset under 40 years of age (particularly in focal hand dystonia and musician’s dys- ...
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Adult Onset Still’s Disease: Articular Manifestations in Twenty Cases
... The adult onset Still’s disease is a rare inflammatory pathology of unknown ...complicating adult onset Still’s disease to define epidemiological, clinical and evolving characteristics of ...
5
Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD
... Neuronal ceroid lipofuscinoses (NCLs) are inherited, progressive, neurodegenerative, lyso- somal storage diseases. Adult-onset NCLs (ANCLs), also known as Kufs disease (KD), are rare and challenging to ...
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Can MR Imaging Diagnose Adult Onset Alexander Disease?
... and adult-onset cases, becoming limited to the lower brain stem and cervical spinal cord ...the adult MR pattern involves a very restricted area at the brain stem-spinal cord junction is ...with ...
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Adult Onset Adrenoleukodystrophy with Frontal Lobe Symptoms: A Case Report
... H-MR spectroscopy (H-MRS) of the white matter in the frontal lobes revealed an extreme decrease of N-acetylaspartate (NAA). An increase in the choline (Cho)/creatinine (Cr) ratio was also found (Figure 2). There was ...
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Adult Onset Cerebral X Linked Adrenoleuokodystrophy in 18 Cases
... utility, however, there is considerable overlap among adult-onset leukodystrophies. Thus, the predictive value of even more sophisticated MRI techniques is limited and there is still an essential need for ...
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Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD
... Citation: van der Zee, J., Marien, P., Crols, R., Van Mossevelde, S., Dillen, L., Perrone, F., Engelborghs, S., Verhoeven, J., D'aes, T., Ceuterick-De Groote, C., Sieben, A., Versijpt, J., Cras, P., Martin, J-J. and Van ...
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Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD
... Neuronal ceroid lipofuscinoses (NCLs) are inherited, progressive, neurodegenerative, lyso- somal storage diseases. Adult-onset NCLs (ANCLs), also known as Kufs disease (KD), are rare and challenging to ...
7