Moebius syndrome in Kallmann syndrome
A. E. Rubinstein, R. E. Lovelace, M. M. Behrens and L. A. Weisberg
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).
