KID-SYNDROME, PACHYDERMATOGLYPHY AND DAND Y-WALKERS SYNDROME

We report a case of KID syndrome in a young girl born to non-consangin ous parents without any similar family history. The typical features o f this dysplasia, erythrokeratodermia with dry rugous teguments, pachy dermia folds of the knees, facial erythema, peribuccal grooves, leucok eratosic perleche, hypotrichosis of the eye lashes and eyebrows, early onset deafness and ophtalmological lesions were observed. The charact eristic pachydermatoglyphia of the hands was present. A malformation o f the posterior cerebral fossa - a dandy walker syndrome - was reveale d at computed tomography.