• In this communication, we describe the otologic and audiometric findings of a rare congenital syndrome associated with profound hearing loss. We offer a hypothesis of the possible inner ear pathologic condition. The major anomalies of this syndrome represent features of an ectodermal dysplasia syndrome.
(Arch Otolaryngol 105:222-224, 1979)
Sismanis A, Polisar IA, Ruffy ML, Lambert JC. Rare Congenital Syndrome Associated With Profound Hearing Loss. Arch Otolaryngol. 1979;105(4):222–224. doi:10.1001/archotol.1979.00790160056015
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