Retinitis pigmentosa not associated with systemic disease (Q99761): Difference between revisions

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Trata-se de uma doença ocular degenerativa hereditária que causa grave comprometimento de visão e frequentemente cegueira. A progressão da RP não é consistente. Algumas pessoas apresentarão sintomas desde a primeira infância, outras podem não perceber os sintomas até mais tarde na vida. Geralmente, quanto mais tardio o início, mais rápida é a deterioração da visão. Esse diagnóstico não está associado a uma doença que afete vários órgãos e tecidos ou afete o corpo como um todo.
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This is an inherited, degenerative eye disease that causes severe vision impairment and often blindness. The progress of RP is not consistent. Some people will exhibit symptoms from infancy, others may not notice symptoms until later in life. Generally, the later the onset, the more rapid is the deterioration in sight. This diagnosis is not associated with a disease that affects a number of organs and tissues, or affects the body as a whole.

Revision as of 16:26, 16 August 2026

This is an inherited, degenerative eye disease that causes severe vision impairment and often blindness. The progress of RP is not consistent. Some people will exhibit symptoms from infancy, others may not notice symptoms until later in life. Generally, the later the onset, the more rapid is the deterioration in sight. This diagnosis is not associated with a disease that affects a number of organs and tissues, or affects the body as a whole.
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    Retinitis pigmentosa not associated with systemic disease
    This is an inherited, degenerative eye disease that causes severe vision impairment and often blindness. The progress of RP is not consistent. Some people will exhibit symptoms from infancy, others may not notice symptoms until later in life. Generally, the later the onset, the more rapid is the deterioration in sight. This diagnosis is not associated with a disease that affects a number of organs and tissues, or affects the body as a whole.

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