Galloway Mowat syndrome (Q104702): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
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). | |||
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 |
|---|---|---|---|
| default for all languages | ID_1140537618 |
||
| 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). |
