Journal
JOURNAL OF CHILD NEUROLOGY
Volume 26, Issue 4, Pages 510-517Publisher
SAGE PUBLICATIONS INC
DOI: 10.1177/0883073810383982
Keywords
Galloway-Mowat syndrome; autopsy; microcephaly; nephrotic syndrome; seizures
Categories
Ask authors/readers for more resources
Galloway-Mowat syndrome is a rare condition that is likely hereditary though the underlying offending gene has not been identified, and is characterized by microcephaly and severe nephrotic syndrome culminating in childhood death. Some of the reported cases have abnormalities in neuronal migration and intractable seizures, but many of the described cases focus on the renal pathology and emphasize a diversity of clinical and pathological features. The case described herein includes a thorough neuropathological description, and when the neuroradiology and neuropathology of the previously published cases is scrutinized, a fairly consistent clinical and neuropathological phenotype emerges.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available