Keratitis, Ichthyosis, Deafness [KID] syndrome with acanthosis nigricans; A case report and review of the literature
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
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Deafness
/
Acanthosis Nigricans
/
Ichthyosis
/
Keratitis
Type of study:
Case report
Limits:
Female
/
Humans
Language:
English
Journal:
Iran. J. Med. Sci.
Year:
1996
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