Infantile Neuroaxonal Dystrophy (INAD): Symptoms Prognosis Children with infantile neuroaxonal dystrophy (INAD) inherit a gene mutation that causes lipids to build up on nerves This rare lipid storage disorder affects your child’s vision, motor skills and development
Infantile Neuroaxonal Dystrophy - National Institute of Neurological . . . Infantile neuroaxonal dystrophy (INAD) is a rare, brain condition that affects the nervous system in young children INAD damages axons—the long parts of nerve cells that carry messages from the brain to other parts of the body
Infantile neuroaxonal dystrophy: MedlinePlus Genetics Infantile neuroaxonal dystrophy is a disorder that primarily affects the nervous system Individuals with infantile neuroaxonal dystrophy typically do not have any symptoms at birth, but between the ages of about 6 and 18 months they begin to experience delays in acquiring new motor and intellectual skills, such as crawling or beginning to speak
Infantile Neuroaxonal Dystrophy: Diagnosis and Possible . . . - Frontiers Infantile neuroaxonal dystrophy (INAD) is an autosomal recessive rare neurodegenerative disease of unknown frequency The onset of symptoms generally occurs between 6 months and 3 years of age Prior to that time, infants develop normally
Infantile Neuroaxonal Dystrophy - BrainFacts Infantile neuroaxonal dystrophy (INAD) is a rare inherited neurological disorder It affects axons, the part of a nerve cell that carries messages from the brain to other parts of the body, and causes progressive loss of vision, muscular control, and mental skills
INADCure - Funding Research and Raising Awareness for INAD The INADcure Foundation is a 501c3 nonprofit charity whose mission is to support the development of treatments, including a cure, for Infantile Neuroaxonal Dystrophy (INAD) and other forms of PLA2G6-related neurodegeneration (PLAN)