Alexander disease infantile form (Q89683): Difference between revisions
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| description / pt-br | description / pt-br | ||
Transtorno neurodegenerativo que ocorre nos primeiros dois anos de vida, com características comuns como megalencefalia, algumas vezes hidrocefalia, atraso do desenvolvimento psicomotor ou declínio cognitivo, sinais piramidais, ataxia e crises convulsivas. | |||
| description / en | description / en | ||
Neurodegenerative disorder occurring within the first two years of life, with common characteristics including megalencaphaly, sometimes hydrocephaly, retarded psychomotor development or mental deterioration, pyramidal signs, ataxia and convulsive seizures. | |||
Revision as of 16:30, 15 August 2026
Neurodegenerative disorder occurring within the first two years of life, with common characteristics including megalencaphaly, sometimes hydrocephaly, retarded psychomotor development or mental deterioration, pyramidal signs, ataxia and convulsive seizures.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1074952784 |
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| English | Alexander disease infantile form |
Neurodegenerative disorder occurring within the first two years of life, with common characteristics including megalencaphaly, sometimes hydrocephaly, retarded psychomotor development or mental deterioration, pyramidal signs, ataxia and convulsive seizures. |
