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Article
July 1975

Moebius Syndrome in Kallmann Syndrome

Author Affiliations

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

Arch Neurol. 1975;32(7):480-482. doi:10.1001/archneur.1975.00490490084010
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).

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