Moebius Syndrome in Kallmann Syndrome

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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