Galloway Mowat syndrome (Q104702): Difference between revisions
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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 |
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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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