Clinical Observation of a Child with KID (Keratitis-Ichthyosis-Deafness) Syndrome

A clinical case of keratitis-ichthyosis-deafness (KID syndrome) in an infant is described. The article familia-rizes pediatricians and family doctors with difficulties in the diagnosis of this rare genetic disease in infants.

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Veröffentlicht in:Zdorovʹe rebenka 2015-09, Vol.10 (6.66), p.129-132
Hauptverfasser: V.A. Klymenko, O.P. Zdybska, T.V. Sirenko, O.M. Plakhotna, N.R. Viun
Format: Artikel
Sprache:eng
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Zusammenfassung:A clinical case of keratitis-ichthyosis-deafness (KID syndrome) in an infant is described. The article familia-rizes pediatricians and family doctors with difficulties in the diagnosis of this rare genetic disease in infants.
ISSN:2224-0551
2307-1168
DOI:10.22141/2224-0551.6.66.2015.75032