spastic ataxia 7 https://www.malacards.org/card/spastic_ataxia_7 https://www.malacards.org/card/spastic_ataxia_7_autosomal_dominant DOID:0050945 SCTID:763669001 GARD:0016560 spastic ataxia 7, autosomal dominant MESH:C566247 MONDO:0007165 spastic ataxia type 7 SPAX7 Spastic ataxia with congenital miosis is a rare hereditary ataxia characterized by an apparently non-progressive or slowly progressive symmetrical ataxia of gait, pyramidal signs in the limbs, spasticity and hyperreflexia (especially in the lower limbs) together with dysarthria and impaired pupillary reaction to light, presenting as a fixed miosis (with pupils that seldom exceed 2 mm in diameter and dilate poorly with mydriatics). Nystagmus may also be present. Orphanet:1182 MEDGEN:354750 autosomal dominant spastic ataxia type 7 OMIM:108650 UMLS:C1862441 autosomal dominant spastic ataxia