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6.
Arch Otolaryngol ; 105(4): 222-4, 1979 Apr.
Article in English | MEDLINE | ID: mdl-426713

ABSTRACT

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.


Subject(s)
Deafness/etiology , Lipase/deficiency , Lipid Metabolism, Inborn Errors/complications , Malabsorption Syndromes/complications , Abnormalities, Multiple , Child, Preschool , Humans , Male
13.
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