SQSTM1 and Dysmetria: The query results show that SQSTM1 has previously been linked to several phenotypes associated with NGLY1 Deficiency, including ‘Cerebellum atrophy’, ‘peripheral nervous system disease’ or interestingly ‘Dysmetria’, a phenotype caused by lesions in the cerebellum or proprioceptive nerves that lead to the cerebellum that coordinate visual, spatial and other sensory information with motor control (53).