Familial 'sleep apnea plus' syndrome: report of a family.

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

Neurology

journal_title

Neurology

authors

Manon-Espaillat R,Gothe B,Adams N,Newman C,Ruff R

doi

10.1212/wnl.38.2.190

subject

Has Abstract

pub_date

1988-02-01 00:00:00

pages

190-3

issue

2

eissn

0028-3878

issn

1526-632X

journal_volume

38

pub_type

杂志文章
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