Galloway-Mowat Syndrome: A condition which is characterized by microcephaly, hiatal hernia and nephrotic syndrome. More detailed information about the symptoms, causes, and treatments of Galloway-Mowat Syndrome is available below.
See full list of 14 symptoms of Galloway-Mowat Syndrome
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Research the causes of these diseases that are similar to, or related to, Galloway-Mowat Syndrome:
Commonly undiagnosed diseases in related medical categories:
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Types of Galloway-Mowat Syndrome
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A syndrome of microcephaly, gyral abnormalities, psychomotor retardation, and glomerulopathy. Seizures, facial defects, hiatus hernia, and other disorders may be associated. - (Source - Diseases Database)
Galloway-Mowat Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Galloway-Mowat Syndrome, or a subtype of Galloway-Mowat Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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