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NEUROLOGY 1988;38:190
© 1988 American Academy of Neurology

Familial 'sleep apnea plus' syndrome

Report of a family

R. Manon-Espaillat, MD, B. Gothe, MD, N. Adams, PhD, C. Newman, PhD and R. Ruff, MD, PhD

From the Departments of Neurology (Drs. Manon-Espaillat, Adams, Newman, and Ruff) and Medicine (Dr. Gothe), Cleveland VA Medical Center and Case Western Reserve University, Cleveland, OH.

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.

Address correspondence and reprint requests to Dr. Manon-Espaillat, VA Medical Center 127W, 10701 East Boulevard, Cleveland, OH 44106.

Received February 6, 1987. Accepted for publication in final form May 29, 1987.




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