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  • Infantile Neuroaxonal Dystrophy (INAD) - Cleveland Clinic
    What is infantile neuroaxonal dystrophy (INAD)? Infantile neuroaxonal dystrophy (INAD) is a rare disease that causes fat substances (lipids) to build up on nerves It affects nerve signals, leading to a gradual loss of muscle control, vision, speech and intellectual development
  • Infantile Neuroaxonal Dystrophy | National Institute of Neurological . . .
    Infantile neuroaxonal dystrophy (INAD) is a rare, inherited disorder of the body’s nervous system It affects axons, the part of a neuron (nerve cell) that carries messages from the brain to other parts of the body
  • Infantile neuroaxonal dystrophy - Wikipedia
    Infantile neuroaxonal dystrophy (INAD) is a rare pervasive developmental 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
  • Understanding INAD – INADCure Foundation
    Infantile Neuroaxonal Dystrophy (INAD) is a rare, autosomal recessive, neurodegenerative disorder that affects young children, causing a progressive loss of motor and cognitive skills
  • Infantile Neuroaxonal Dystrophy (INAD) - Rare Genomics Institute
    Infantile neuroaxonal dystrophy (INAD) is a rare, genetic neurological disorder Symptoms usually present between 6 and 18 months of age There is often rapid onset of motor and intellectual regression
  • inadwarriors. org
    Infantile Neuroaxonal Dystrophy (INAD) is an ultra-rare (<200 worldwide) inherited neurodegenerative disorder It destroys axons, the part of the neuron (nerve cell) that carries messages from the brain to other parts of the body through build up of fatty substances (lipids) on the nerves
  • The infantile neuroaxonal dystrophy rating scale (INAD-RS)
    INAD is an autosomal recessive neurogenetic disorder caused by biallelic pathogenic variants in PLA2G6 The downstream enzyme, iPLA 2, plays a critical role in cell membrane homeostasis by helping to regulate levels of phospholipids
  • Infantile neuroaxonal dystrophy - MedlinePlus
    Infantile neuroaxonal dystrophy is characterized by the development of swellings called spheroid bodies in the axons, the fibers that extend from nerve cells (neurons) and transmit impulses to muscles and other neurons
  • INAD | NBIA - NBIAcure
    The symptoms of INAD (infantile neuroaxonal dystrophy) usually start to appear between the ages of 6 months and 1 year A common pattern in young children is loss of skills and progression of the disorder over time
  • Frontiers | Infantile Neuroaxonal Dystrophy: Diagnosis and Possible . . .
    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





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