Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3037588 | Brain and Development | 2011 | 4 Pages |
Abstract
Congenital infection-like syndrome includes multiple disorders. Although novel syndromes have recently been described and their genetic defects identified, many cases remain unclassified. Here we report a patient with neuroradiologic findings of intracranial calcification and cerebellar hypoplasia, and clinical features of growth retardation, progressive pancytopenia, interstitial pneumonia, and immune abnormality. Our patient had a phenotypic overlap with Aicardi-Goutières syndrome and Hoyeraal-Hreidarsson syndrome, despite the absence of mutation in their responsible genes.
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Authors
Yoko Mizuno, Kan Takahashi, Takashi Igarashi, Makiko Saito, Masashi Mizuguchi,