ATROFIA MUSCULAR ESPINHAL PROGRESSIVA PDF

ATROFIA MUSCULAR ESPINHAL PROGRESSIVA PDF

May 12, 2020 Technology by admin

Twelve children with progressive spinal muscular atrophy were seen at Santo Antonio Children Hospital, Porto Alegre. Diagnosis was based on neurological. diagnosticada com Atrofia Muscular Espinhal (AME) do tipo 1, uma doença severa e progressiva que degenera os neurônios motores, inclusive da respiração. 17 nov. O presente trabalho aborda sobre a atrofia muscular espinhal (AME), também denominada amiotrofia muscular espinhal, que consiste em uma.

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Dysphagia was the main gastroenterological complication. The authors conclude progresssiva the lack of acquisition of motor developmental milestones is correlated to worse vital and functional prognosis.

Remédio inédito para atrofia muscular espinhal é liberado

Several types of the disease have been described along with several classification systems based either on the age at onset of symptoms or on the maximum function achieved. Users should refer to the original published version of the material for the full abstract.

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This abstract may be abridged. All patients sustained recurrent lower respiratory infections during the course of the disease.

SMA leads to a vast group of secondary manifestations in various organ systems, particularly the respiratory, muscle-skeletal and gastrointestinal. An inverse relation was found between the progresskva of the course of illness and the age at onset and maximum motor function achieved.

English Copyright of Acta Medica Portuguesa is the property of Centro Editor Livreiro da Ordem dos Medicos CELOM espunhal its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder’s express written progressica. However, remote access to EBSCO’s databases from non-subscribing institutions is not allowed if the purpose of the use is for commercial gain through cost reduction or avoidance for a non-subscribing institution.

The authors conducted a retrospective study focusing on socio-demographic, clinical parameters, evolution and complications of the disease.

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Atrofia muscular espinhal infantil progressiva relato de 12 casos

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The main musculoskeletal complication was the development of contractures in the main joints of the lower limbs, as well as scoliosis. Respiratory insufficiency complicated by cardio-respiratory arrest was the cause of death in the deceased patients. It is genetically determined, with the absence or mutation of the muscylar motor neuron 1 SMN1 as a hallmark.

Spinal Muscular atrophy SMA ewpinhal a genetically determined specific neuromuscular disease, characterized by the deterioration of spinal a motor neurons, causing progressive muscular atrophy and weakening.