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IJMS-Iranian Journal of Medical Sciences. 1996; 21 (3-4): 176-178
in English | IMEMR | ID: emr-41149

ABSTRACT

We report a case of KID syndrome in a 14-year-old girl with a negative family history. The typical features of this syndrome, ichthyosis, hypotrichosis of the eyelashes and eyebrows, neurosensory deafness and keratitis were observed. Another finding in this patient was benign acanthosis nigricans, which is reported here for the first time in association with KIDS


Subject(s)
Humans , Female , Keratitis , Ichthyosis , Deafness , Acanthosis Nigricans
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