Hypospasdias  intellectual deficit, Goldblatt type is a very rare multiple congenital anomalies syndrome described in three brothers of one South-African family, and characterized by hypospadias and intellectual deficit, in association with mirocephaly, craniofacial dysmorphism, joint laxity and beaked nails. The disease is Orphanet rare-disease nomenclature id Orphanet_2261 (Hypospadias - intellectual disability, Goldblatt type). Also known as: Goldblatt-Wallis syndrome.