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Allen E. Rubinstein, MD; Robert E. Lovelace, MD; Miles M. Behrens, MD; Leon A. Weisberg, MD

Arch Neurol. 1975;32(7):480-482.

Abstract
A girl born with congenital paresis of cranial nerves III, IV, and VII (Moebius syndrome) subsequently developed a progressive peripheral neuropathy. There was suggestive evidence of a familial neuropathy with autosomal dominant inheritance in three family members. The patient also had hypogonadotrophic hypogonadism and anosmia (Kallmann syndrome).

Author Affiliations
From the departments of neurology and ophthalmology, Columbia University College of Physicians and Surgeons, New York.

Footnotes
Accepted for publication Oct 21, 1974.

Reprint requests to Department of Neurology, Mount Sinai School of Medicine, 100th St and Fifth Ave, New York, NY 10029 (Dr. Rubinstein).

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