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641 Possible Causes for Neuroaxonal Dystrophy

  • Hallervorden-Spatz Syndrome

    Dystrophy, Juvenile-Onset edit English pantothenate kinase-associated neurodegeneration A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal[wikidata.org] The clinical and pathological features, including electron microscopy of a sporadic case of neuroaxonal dystrophy with findings of both Hallervorden-Spatz syndrome (HS) and[ncbi.nlm.nih.gov] The changes are compared to those in a case of infantile neuroaxonal dystrophy (Seitelberger's disease), the first to be reported in Scandinavia.[doi.org]

  • Infantile Neuroaxonal Dystrophy

    The relationship of these features to the symptoms of infantile neuroaxonal dystrophy is unknown. Infantile neuroaxonal dystrophy is a very rare disorder.[ghr.nlm.nih.gov] neuroaxonal dystrophy Phospholipase A2-associated neurodegeneration INAD1 edit English Infantile neuroaxonal dystrophy No description defined infantile neuroaxonal dystrophy[wikidata.org] Infantile neuroaxonal dystrophy may be classical or atypical.[symptoma.com]

  • Infantile Neuroaxonal Dystrophy 1

    Infantile Neuroaxonal Dystrophy, a rare genetic neurological disorder.[disabilitybenefitscenter.org] Image: Getty Read more articles on Infantile Neuroaxonal Dystrophy.[onlymyhealth.com] INAD (Infantile Neuroaxonal Dystrophy) is a rare heredo-degenerative disease with onset in early infancy (after a period of latency), clinically characterized by progressive[moh-it.pure.elsevier.com]

  • Neurodegeneration with Brain Iron Accumulation

    More recently, it was found that mutations in the PLA2G6 gene cause both infantile neuroaxonal dystrophy (INAD) and, more rarely, an atypical neuroaxonal dystrophy that overlaps[ncbi.nlm.nih.gov] Clinical description NBIA can present as early onset with rapid progression: classic pantothenate kinase-associated neurodegeneration (PKAN), infantile neuroaxonal dystrophy[orpha.net] Neurodegeneration with Brain Iron Accumulation (NBIA) is a rare type of neuroaxonal dystrophy that can be familial or sporadic, characterized by progressive extrapyramidal[ncbi.nlm.nih.gov]

  • Schindler Disease

    […] in the other neuroaxonal dystrophies, results from abnormal glycoprotein metabolism involving O-linked glycopeptides.[ncbi.nlm.nih.gov] Schindler disease is a recently recognized infantile neuroaxonal dystrophy resulting from the deficient activity of the lysosomal hydrolase, alpha-N-acetylgalctosaminidase[ncbi.nlm.nih.gov] A neuroaxonal dystrophy due to lysosomal α - N -acetylgalactosaminidase deficiency. N. Engl. J.[link.springer.com]

  • Kanzaki Disease

    Type 1 is characterized by infantile-onset neuroaxonal dystrophy, type 2 is described in adult patients with angiokeratoma corporis diffusum and minimal involvement of the[orpha.net] dystrophy (Schindler disease) and late onset angiokeratoma corporis diffusum (Kanzaki disease).[ncbi.nlm.nih.gov] dystrophy resulting from the deficient activity of the lysosomal hydrolase, alpha-N-acetylgalctosaminidase (alpha-GalNAc).[doi.org]

  • Diabetic Autonomic Neuropathy

    Two months of IGF-I treatment of chronically diabetic rats with established neuroaxonal dystrophy (the neuropathological hallmark of the disease) involving the superior mesenteric[ncbi.nlm.nih.gov] The basic neurobiologic process underlying the diabetes-induced development of neuroaxonal dystrophy, synaptic dysplasia, defective axonal regeneration, and alterations in[ncbi.nlm.nih.gov] Neuroaxonal dystrophy (NAD), a distinctive axonopathy involving distal axons and synapses, represents the neuropathologic hallmark of diabetic sympathetic autonomic neuropathy[ncbi.nlm.nih.gov]

  • Nivelon-Nivelon-Mabille Syndrome

    dystrophy renal tubular acidosis Neuroaxonal dystrophy, late infantile Neuroectodermal endocrine syndrome Neuroectodermal tumors primitive Neuroendocrine carcinoma of the[mindmappedia.com] dystrophy renal tubular acidosis Neuroaxonal dystrophy, late infantile Neuroblastoma Neurocutaneous melanosis Neuroectodermal endocrine syndrome Neuroectodermal tumors primitive[bionity.com] Eichner Opitz syndrome Neural tube defect, folate-sensitive Neural tube defects X linked Neuraminidase beta-galactosidase deficiency Neuritis with brachial predilection Neuroaxonal[mindmappedia.com]

  • Beta-Propeller Protein-Associated Neurodegeneration

    We enrolled 28 patients with childhood intellectual disability and young-onset parkinsonism ( 40 years at onset) and 4 patients with infantile neuroaxonal dystrophy.[ncbi.nlm.nih.gov] A case of infantile neuroaxonal dystrophy of neonatal onset. J Child Neurol 2015;30:368-70. [Figure 1][annalsofian.org] The most common of these is classical or infantile-onset phospholipase A2-associated neurodegeneration, also known as infantile neuroaxonal dystrophy (INAD).[annalsofian.org]

  • Alzheimer Disease

    T. (1999) Alpha-synuclein immunoreactivity is present in axonal swellings in neuroaxonal dystrophy and acute traumatic brain injury. J. Neuropathol. Exp.[doi.org]

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