Galloway Mowat syndrome (Q104702): Difference between revisions
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A síndrome de Galloway é caracterizada pela associação de síndrome nefrótica resistente a esteroides e anomalias do sistema nervoso central (microcefalia, atraso psicomotor, convulsões, hipotonia, giros e sulcos cerebrais anormais, atrofia cortical, hidrocefalia devida a estenose aquedutal, porencefalia ou encefalomalácia). | |||||||||||||||
| description / en | description / en | ||||||||||||||
Galloway syndrome is characterised by the association of steroid-resistant nephrotic syndrome and central nervous system anomalies (microcephaly, psychomotor retardation, convulsions, hypotonia, abnormal cerebral giri and sulci, cortical atrophy, hydrocephalus due to aqueductal stenosis, porencephaly or encephalomalacia). | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1140537618 / rank | |||||||||||||||
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CID11:ID_1140537618 | |||||||||||||||
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dki-india-ID_1140537618 | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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16 August 2026
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| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
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Latest revision as of 10:34, 17 August 2026
Galloway syndrome is characterised by the association of steroid-resistant nephrotic syndrome and central nervous system anomalies (microcephaly, psychomotor retardation, convulsions, hypotonia, abnormal cerebral giri and sulci, cortical atrophy, hydrocephalus due to aqueductal stenosis, porencephaly or encephalomalacia).
| Language | Label | Description | Also known as |
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| default for all languages | ID_1140537618 |
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| English | Galloway Mowat syndrome |
Galloway syndrome is characterised by the association of steroid-resistant nephrotic syndrome and central nervous system anomalies (microcephaly, psychomotor retardation, convulsions, hypotonia, abnormal cerebral giri and sulci, cortical atrophy, hydrocephalus due to aqueductal stenosis, porencephaly or encephalomalacia). |
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CID11:ID_1140537618
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dki-india-ID_1140537618
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Concluído
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16 August 2026
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