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KID syndrome: About a case
Nasza Dermatologia Online
KID syndrome is a rare autosomal dominant genetic disorder, due to a lack of keratinization. Rarely sporadic. It is manifested by the main triad; keratitis ictyosis and deafness. cutaneous manifestations are detected at birth or a little later in the neonatal period, while ocular and auditory manifestations are later detected during childhood or adolescence to varying degrees, although they are present at the birth. The management of this pathology is difficult with a risk of deafness generallydoi:10.7241/ourd.2020e.45 fatcat:fsglho677zcodmt7cwjqypfiii