Sialidosis type 1 (Q97048): Difference between revisions

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A sialidose tipo 1, também chamada de normomórfica ou 'mancha vermelha-cereja, síndrome de mioclonia' é uma forma de sialidose, uma doença de depósito lisossomal. Pertence ao grupo das oligossacaridoses ou glicoproteinoses, e é caracterizada por dificuldades de locomoção e/ou perda de acuidade visual e uma mancha vermelho-cereja na retina. Podem ocorrer mioclonia generalizada, em alguns casos associada a convulsões.
description / endescription / en
 
Type 1 sialidosis, also called normomorphic or 'cherry-red-spot, myoclonus' syndrome is a form of sialidosis, a lysosomal storage disease belonging to the group of oligosaccharidoses or glycoproteinoses, and is characterised by walking difficulties and/or a loss of visual acuity and a cherry-red spot on the retina. They may also have generalised myoclonus, in some cases associated with seizures.
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Property / Canonical URI: https://id.who.int/icd/entity/1154773192 / rank
 
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CID11:ID_1154773192
Property / CURIE: CID11:ID_1154773192 / rank
 
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dki-india-ID_1154773192
Property / Canary Token: dki-india-ID_1154773192 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 13:04, 16 August 2026

Type 1 sialidosis, also called normomorphic or 'cherry-red-spot, myoclonus' syndrome is a form of sialidosis, a lysosomal storage disease belonging to the group of oligosaccharidoses or glycoproteinoses, and is characterised by walking difficulties and/or a loss of visual acuity and a cherry-red spot on the retina. They may also have generalised myoclonus, in some cases associated with seizures.
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ID_1154773192
    English
    Sialidosis type 1
    Type 1 sialidosis, also called normomorphic or 'cherry-red-spot, myoclonus' syndrome is a form of sialidosis, a lysosomal storage disease belonging to the group of oligosaccharidoses or glycoproteinoses, and is characterised by walking difficulties and/or a loss of visual acuity and a cherry-red spot on the retina. They may also have generalised myoclonus, in some cases associated with seizures.

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      CID11:ID_1154773192
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      dki-india-ID_1154773192
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      Concluído
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      15 August 2026
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