Abstract:
:We describe a familial disorder consisting of sleep apnea, anosmia, colorblindness, partial complex seizures, and cognitive dysfunction. The phenotypic expression of the syndrome suggests an autosomal dominant inheritance with incomplete penetrance.
journal_name
Neurologyjournal_title
Neurologyauthors
Manon-Espaillat R,Gothe B,Adams N,Newman C,Ruff Rdoi
10.1212/wnl.38.2.190subject
Has Abstractpub_date
1988-02-01 00:00:00pages
190-3issue
2eissn
0028-3878issn
1526-632Xjournal_volume
38pub_type
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