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galloway
/ˈɡæləˌweɪ/
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mowat
/moʊət/
syndrome
/ˈsɪnˌdroʊm/
Description
Galloway-Mowat syndrome    autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome

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