Galloway Mowat syndrome (Q104702)

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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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ID_1140537618
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    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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