Galloway Mowat syndrome (Q104702): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
16 August 2026
| |||||||||||||||
| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
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 |
|---|---|---|---|
| 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). |
Statements
CID11:ID_1140537618
0 references
dki-india-ID_1140537618
0 references
Concluído
0 references
16 August 2026
0 references
