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).
Rubinstein AE, Lovelace RE, Behrens MM, Weisberg LA. Moebius Syndrome in Kallmann Syndrome. Arch Neurol. 1975;32(7):480–482. doi:10.1001/archneur.1975.00490490084010
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