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1.
Indian J Med Microbiol ; 2016 Oct-Dec; 34(4): 550-553
Article Dans Anglais | IMSEAR | ID: sea-181136

Résumé

Fungal brain abscess is rare with a rapidly progressive disease with fulminant course and invariably fatal outcome, unless diagnosed early and treated rapidly. We report a 56‑year‑old woman diagnosed to have fungal abscess who recovered completely following amphotericin B treatment. She presented with weakness of the right hand, deviation of mouth to left and aphasia for 2 days. Computed tomography of the brain revealed a left frontal capsuloganglionic hypodense lesion. Stereotactic biopsy was performed, and microbiological confirmation of non‑septate fungal hyphae from pus from aspirate within 2 h helped initiate timely and appropriate treatment leading to cure. Histopathology and culture later confirmed mucormycosis.

4.
Indian J Pediatr ; 2010 Feb; 77(2): 193-195
Article Dans Anglais | IMSEAR | ID: sea-142499

Résumé

Case records of female patients with karyotype proven turner syndrome were analyzed. 11 patients had classic Turner karyotype (Group 1) and 13 patients had karyotype suggestive of one of the variants of Turner syndrome (Group 2). There was a median difference of 3 years between the age of presentation and the age of diagnosis in Group 2. Out of the thirteen patients in Group 2, 4 had no clinical stigmata of Turner Syndrome; the rest (n=9) had one or more of the typical clinical stigmata of Turner Syndrome. One patient with a complex mosaic karyotype also had an intracranial medulloblastoma. One patient in each group had coarctation of the aorta. 5 patients in Group 1 and 3 patients in Group 2 had primary hypothyroidism and received levothyroxine. The median Thyroid Stimulating Hormone levels were significantly higher among patients in group 1 than in group 2.


Sujets)
Adolescent , Femelle , Variation génétique/génétique , Hormone de croissance/usage thérapeutique , Humains , Hypothyroïdie/sang , Hypothyroïdie/traitement médicamenteux , Caryotypage , Thyréostimuline/sang , Thyroxine/usage thérapeutique , Syndrome de Turner/diagnostic , Syndrome de Turner/traitement médicamenteux , Syndrome de Turner/génétique
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