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1.
Schweiz Med Wochenschr ; 130(44): 1689-91, 2000 Nov 04.
Artículo en Inglés | MEDLINE | ID: mdl-11103442

RESUMEN

Familial hypokalaemic periodic paralysis is an autosomal dominant muscle disease which has been linked to point mutations in the skeletal muscle L-type calcium channel alpha 1 subunit (alpha 1 s). It consists of muscular weakness episodes due to hypokalaemia caused by intracellular shifting of potassium. We describe the case of a young man of Kurdish origin, with a history of Graves' disease, who was admitted to the emergency room with hypotonic tetraplegia associated with severe hypokalaemia.


Asunto(s)
Enfermedad de Graves/complicaciones , Parálisis Periódica Hipopotasémica/complicaciones , Adulto , Antitiroideos/uso terapéutico , Carbimazol/uso terapéutico , Urgencias Médicas , Enfermedad de Graves/diagnóstico , Enfermedad de Graves/tratamiento farmacológico , Humanos , Masculino , Cuadriplejía/etiología , Suiza , Turquía/etnología
3.
Pediatrie (Bucur) ; 41(1): 71-4, 1992.
Artículo en Rumano | MEDLINE | ID: mdl-1322730

RESUMEN

The present paper concerns the problem of nifedipine poisoning at a 2-year- [correction of 1-year-] and 4-month-old boy, developed after ingestion of 15 tablets with 150 mg active substance. The medical care was represented by: a) gastric lavage with evacuation of stomach content and b) repeated administration of calcium with permanent monitoring of cardiac rhythm, electrocardiography and blood pressure. The evolution was very good with total disappearance of clinical signs in first 6 hours after admission.


Asunto(s)
Nifedipino/envenenamiento , Preescolar , Urgencias Médicas , Humanos , Lactante , Masculino , Intoxicación/diagnóstico , Intoxicación/terapia , Comprimidos
4.
Pediatrie (Bucur) ; 40(1-2): 163-8, 1991.
Artículo en Rumano | MEDLINE | ID: mdl-1667597

RESUMEN

On the basis of the present knowledge in the nephrotic syndrome with minimum glomerular lesions, the paper reviews the paradoxes of the disease: the glomeruli with normal histologic structure in optic microscopy, but with the highest proteinuria in the whole human pathology; absence of some clear arguments concerning the existence of the immunologic disorders, but the best medication is corticotherapy and immunodepressive drugs; the high incidence of the allergic background against which the nephrotic syndrome appears, but with or without a limited effect of the antiallergic medication. The above-mentioned elements may be interesting research fields in the future.


Asunto(s)
Nefrosis Lipoidea/diagnóstico , Niño , Humanos , Glomérulos Renales/patología , Nefrosis Lipoidea/patología , Proteinuria/diagnóstico , Proteinuria/patología
5.
Pediatrie (Bucur) ; 39(2): 173-5, 1990.
Artículo en Rumano | MEDLINE | ID: mdl-1966514

RESUMEN

The paper reports on a case of chronic pyelonephritis with bacillus Proteus, generated by an intravesical foreign body (sewing needle). The needle was extracted with surgical cystoscope. After removing the foreign body, nalidixic acid was administered. The immediate evolution of the case was good.


Asunto(s)
Cuerpos Extraños/complicaciones , Pielonefritis/etiología , Vejiga Urinaria , Niño , Enfermedad Crónica , Terapia Combinada , Cistoscopía , Femenino , Cuerpos Extraños/diagnóstico , Cuerpos Extraños/terapia , Humanos , Ácido Nalidíxico/administración & dosificación , Agujas , Infecciones por Proteus/diagnóstico , Infecciones por Proteus/tratamiento farmacológico , Infecciones por Proteus/etiología , Pielonefritis/diagnóstico , Pielonefritis/tratamiento farmacológico
8.
Artículo en Rumano | MEDLINE | ID: mdl-2505364

RESUMEN

The authors described the clinical, biologic and histologic particularities of two cases of congenital nephrotic syndrome, Finnish type. Clinically, the hydropic syndrome was represented by anasarca: biologically by marked proteinuria, hypoproteinemia with dysproteinemia and hyperlipemia with dyslipemia. Histologically both cases presented microcystic dilatation of the proximal tubuli contorti. The evolution was unfavorable and ended in death.


Asunto(s)
Síndrome Nefrótico/congénito , Femenino , Humanos , Lactante , Riñón/patología , Síndrome Nefrótico/diagnóstico , Síndrome Nefrótico/patología
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