A atrofia muscular espinhal é geralmente diagnosticada com um simples teste de sangue. Se o teste genético não for capaz de confirmar a AME, existem outras formas de ver se o seu filho tem esta doença que torna os músculos fracos.
A fraqueza muscular pode ser um sinal de atrofia muscular espinhal, que pode atingir todas as idades, mas é a causa genética nº 1 de morte em bebés. Eis o que é e o que se pode fazer a esse respeito.
A estimulação cerebral profunda (DBS) é utilizada para tratar uma série de perturbações do movimento, incluindo o tremor essencial. o médico diz-lhe mais.
médico explica os sintomas, possíveis causas, e tratamento do tremor essencial, distúrbio comum do movimento que causa tremores incontroláveis nas extremidades superiores.
A matéria branca compõe a maior parte do seu cérebro. Perde-se muito com a idade. Isso pode causar problemas de pensamento, marcha e equilíbrio. o médico diz-lhe como evitá-lo.
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