Megalocornea and iris anomalies accompanied by facial and skeletal defects, slow psychomotor development, hypotonia, and seizures. Later reports classify megalocornea-mental retardation syndrome into several types: Type 1 Synonym: Neuhauser syndrome With iris hypoplasia and minor abnormalities. Type 2 With camptodactyly, scoliosis, and growth retardation. Type 3 Synonym: Verloes type With macrocephaly, hypotonia, and other minor anomalies but no hypoplasia of the irides. Type 4 With megalocephaly,obesity, and normal irides.
