Moebius syndrome in Kallmann syndrome.

Arch Neurol, 1975/7;32(7):480-2.

Rubinstein AE, Lovelace RE, Behrens MM, Weisberg LA

PMID: 166632

Abstract
A girl born with congenital paresis of cranial nerves III, IV, and VII (Moeblus 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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