Cinco Doenças Raras Que se Escondem Dentro do Olho (2016)

Saiba Quais são as Doenças Raras Que se Escondem Dentro do Olho

Cinco Doenças Raras Que se Escondem Dentro do Olho. Optometristas e oftalmologistas usam um phoropter (aparelho para os olhos) para determinar prescrições de óculos e lentes de contato.

Ao dilatar os olhos, os médicos podem, assim, encontrar as doenças raras.

Se você acredita ou não que os olhos são a janela da alma, não há dúvida de que olhando para os alunos você pode ajudar os médicos a detectar problemas de saúde.

Alguns são sérios e raros e só pode ser detectado quando o seu médico brilha uma luz em seus olhos ou quando o optometrista ou oftalmologista dilata o nervo e as pupilas nos vasos sanguíneos.

As crianças beneficiam de exames oftalmológicos de forma significativa e exames de vista pré-escolar.

Abaixo Estão Cinco Doenças Oftalmológicas Raras Que se Escondem no Fundo dos Olhos.

Doença de Coats é uma doença ocular rara que pode levar à cegueira em um olho.

É causada pelo desenvolvimento anormal dos vasos sanguíneos da retina.

Os sintomas dependem do tamanho e extensão dos vasos sanguíneos afetados, e começam tipicamente entre 6 e 8 anos de idade.

A doença pode causar alguma perda de visão ou inicialmente os olhos pareçam cruzados. A massa branca pode, portanto, se desenvolver no aluno atrás da lente.

Como a doença de Coats progride, os indivíduos podem desenvolver glaucoma, catarata ou manchas avermelhadas na íris.

O globo ocular afetado pode, portanto, diminuir e a camada média do olho e pode se inchar ou tornar-se irritado.

Não se sabe o que causa a Coats, mas investigadores suspeitam que uma ligação genética.

As opções de tratamento são ditadas pela fase da doença quando diagnosticada.

Muitas vezes, os médicos se concentram em fechar os vasos que estão vazando e salvar tanto a visão quanto possível.

No entanto, casos avançados podem exigir cirurgia.

 

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(VÍDEO) Doença de Coats

 

(VÍDEO) Dose de Saúde – O que é Retinoblastoma?

 

(VÍDEO) Doenças da Visão

 

(VÍDEO) Principais Doenças que Afetam a Visão

 

O retinoblastoma é um câncer que traz risco de vida pela retina.

Isso faz com que o aluno apareça em luz branca em vez de luz vermelha. Isto pode ser visto em uma fotografia pelo flash.

Outros sintomas incluem dor ou vermelhidão nos olhos.

Retinoblastoma geralmente afeta crianças menores de 5 anos, e pode afetar um ou ambos os olhos.

Pode-se espalhar para outras áreas em redor do olho, no cérebro ou outras partes do corpo.

Em alguns casos, a doença é hereditária, por isso especialistas recomendam aos pais e irmãos fazer um exame de olho por oftalmologista para ver a formação da doença.

Se diagnosticado precocemente, o tratamento menos intenso pode ser necessário, mas o objetivo principal de uma equipe de cuidado com a criança com câncer é salvar a vida da criança, então a visão, se possível.

Microftalmia é uma desordem que deixa um ou ambos os olhos anormalmente pequenos, enquanto anoftalmia é a ausência de um ou ambos os olhos.

Ambas as condições se desenvolvem durante a gravidez, potencialmente, a partir de uma mutação genética de cromossomos anormais.

Alguns pesquisadores acreditam que a exposição a raios-x, produtos químicos, medicamentos, pesticidas, toxinas, radiação, vírus aumentam o risco de doenças.

Entretanto, a pesquisa não é conclusiva. Às vezes, a causa em um doente individual não pode ser determinada.

Não há tratamento para anoftalmia grave ou microftalmia cria um novo olho ou restaura a visão.

As crianças podem usar um olho artificial para fins cosméticos, mas terão de suportar os confórmeros e fazer a cavidade ocular crescer.

Essa doença é uma forma hereditária de degeneração macular que leva à perda da visão central, que permite que você veja detalhes finos e cores.

Nas fases iniciais da doença, forma-se um quisto amarelo brilhante sob o epitélio pigmentado da retina (RPE) sob a mácula.

Alguns com a doença pode ter visão normal ou quase normal por muitos anos.

Para outros, o cisto eventualmente explode, causando perda de visão. Esta situação geralmente ocorre.

A doença não pode afetar ambos os olhos de forma igual. Muitas pessoas mantêm a visão central útil em um olho.

Atualmente, não há tratamento para a doença.

Atrofia girata afeta a coroide, ou o revestimento fino do olho, e na retina, levando à perda de visão gradual. Cegueira total geralmente ocorre entre as idades de 40 e 60.

A doença é provocada por genes mutantes causados pelo encontro no cromossomo 10.

A investigação mostra, de fato uma dieta de proteína baixa, suplementado com aminoácidos essenciais que podem beneficiar a maioria dos pacientes, retardando a progressão da doença.

Os pesquisadores estão investigando mutações variantes dos genes herdados na esperança de desenvolver uma cura.

medico emagecer mulher azul

 

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