ENFERMEDAD DE GERSTMANN-STRAUSSLER-SCHEINKER PDF

Familiares: Enfermedad de Creutzfeldt – Jacob familiar- Síndrome de Gerstmann – Sträussler – Scheinker- Insomnio familiar fatal- Enfermedades por priones. Gerstmann–Sträussler–Scheinker syndrome (GSS) is an extremely rare, usually familial, fatal De Michele G, Pocchiari M, Petraroli R, et al. (August ). A number sign (#) is used with this entry because of evidence that Gerstmann- Straussler disease (GSD) and a form of cerebral amyloid angiopathy are caused .

Author: Gazilkree Tur
Country: Luxembourg
Language: English (Spanish)
Genre: Life
Published (Last): 17 January 2008
Pages: 313
PDF File Size: 13.97 Mb
ePub File Size: 7.51 Mb
ISBN: 547-3-24760-618-1
Downloads: 12561
Price: Free* [*Free Regsitration Required]
Uploader: Nikobei

Entre las principales variables analizadas figuraron: Only 1 patient had clear dementia on initial examination.

In a year-old woman who belonged to the original family reported by Gerstmann et al. Insuficiencia renal aguda IRA. A change in codon from proline to leucine has been found in the prion protein gene PRNPon chromosome 20 of most affected individuals.

OMIM Entry – # – GERSTMANN-STRAUSSLER DISEASE; GSD

However, all patients developed cortical and diffuse brain atrophy with disease progression and onset of dementia. Impacto social Breast feeding and immunity. Gerstmnan-straussler-scheinker Cubana Med Mil ;35 2: GSS can be identified through genetic testing. Oral Health Promotion in the childhood and adolescence: Early features included impaired smooth pursuit eye movements, impaired short-term memory, and clumsiness of the hands.

Kuru in the 21 st century: Their goal gerstmannn-straussler-scheinker to try to improve the patient’s quality of life as much as possible. No es aplicable cuando se trata de delitos cometidos por imprudencia y el error se debe a la imprudencia misma del agente. Severe pulmonary haemorrhage accompanying hepatorrenal failure in fulminant leptospirosis.

  DEMAG HC810 PDF

Nivel de relaciones interpersonales satisfactorio. Multilevel Statistical ModelsLondon. J Clin Oncol ; Se utiliza de acuerdo con el grado de riesgo identificado de las siguientes formas: Sixty-four patients enfermedae progressive ataxia, dementia, and parkinsonism with onset in the late thirties to early sixties.

Gerstmann–Sträussler–Scheinker syndrome

Saude Bucal do pre-escolares Piracicoba Brasil Y ahora en detalladamente: In each of the generations sinceaffected members had been identified by either history or clinical examination. Rev Cubana Pediatr ;77 1: One of these patients was a member of the family reported by Adam et al.

The creation of a computer program for the evaluation of diagnostic means and the analysis of clinical enfegmedad demanded to investigate cautiously on the current situation in regard to the automation of both processes, all gerstmann-straussler-schfinker which is briefly exposed in this article, where it is stated that the computer treatment of these methods and procedures can be qualified today as disperse and incomplete. El concepto de salud. She was diagnosed with Alzheimer disease, but reexamination of her pathology showed the same abnormalities as observed in her daughter.

Pages using deprecated image syntax Infobox medical condition new.

Dientes perdidos 44, 34, 14 y The Cochran CollaborationOxford Versiones 3. N Engl J ; Provincia Santiago de Cuba, Servicio de Salud Metropolitano Norte. La enfermedad es conocida por diferentes nombres: Seitelberger described a kindred with a gershmann-straussler-scheinker neurologic disorder traced through 5 generations. Other aspects of interest are equally commented, those related to the communicative barriers, the satisfactory and effective communication between patient – relatives and health staff, as well as during the assistance and educational practice.

  BECOMING MEMBERS OF SOCIETY AARON DEVOR PDF

No tratamiento correcto de los procesos. dee

Gerstmann–Sträussler–Scheinker syndrome – Wikipedia

However, therapies and medication are aimed at treating or slowing down the effects of the symptoms. American Journal of Cardiology ;99 11 Suppl 1: Gerstmann-Straussler disease typically presents with progressive limb and gerstmznn-straussler-scheinker ataxia, dysarthria, and cognitive decline in the thirties and forties, and the average disease duration is 7 years. Proclama que un paciente es ante todo un ser humano y no un simple caso. Canadian Medical Association Journal ; 4: The highest incidence rate for inhabitants was registered in II Frente municipality 29,0 and the largest number of cases 64 in Santiago de Cuba municipality.

Cultura general integral 4. The disorder had lasted 8 years.