Fig. 1From: Congenital nephrotic syndrome associated with 22q11.2 duplication syndrome in a Chinese family and functional analysis of the intronic NPHS1 c. 3286 + 5G > A mutationDysmorphic features of the proband. Hypertelorism, palpebral edema, broad nose bridge, upturned nose, dysmorphic auricle, long philtrum, and a thin upper lip. Additionally, left wrist drop and bilateral strephexopodia, bilateral knee joint flexion contractureBack to article page