Keyword Analysis & Research: infantile neuroaxonal dystrophy


Keyword Analysis

Keyword CPC PCC Volume Score Length of keyword
infantile neuroaxonal dystrophy0.590.663334631
infantile1.480.78569229
neuroaxonal1.140.31767411
dystrophy0.620.11630849

Keyword Research: People who searched infantile neuroaxonal dystrophy also searched

Keyword CPC PCC Volume Score
infantile neuroaxonal dystrophy1.780.6986517
infantile neuroaxonal dystrophy icd 100.520.1523570
infantile neuroaxonal dystrophy inad0.330.196652
infantile neuroaxonal dystrophy life span1.810.3939280
infantile neuroaxonal dystrophy case reports0.010.3511828

Search Results related to infantile neuroaxonal dystrophy on Search Engine

  • Infantile Neuroaxonal Dystrophy | National Institute of …

    nih.gov

    https://www.ninds.nih.gov/health-information/disorders/infantile-neuroaxonal-dystrophy

    WEBNov 28, 2023 · 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. INAD causes loss of vision, muscular control, and mental skills. These symptoms get worse as time passes.

    DA: 38 PA: 86 MOZ Rank: 23

  • Infantile Neuroaxonal Dystrophy (INAD): Symptoms & Prognosis

    clevelandclinic.org

    https://my.clevelandclinic.org/health/diseases/22767-infantile-neuroaxonal-dystrophy-inad

    WEBWhat 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 …

    DA: 34 PA: 96 MOZ Rank: 69

  • Infantile neuroaxonal dystrophy - Wikipedia

    wikipedia.org

    https://en.wikipedia.org/wiki/Infantile_neuroaxonal_dystrophy

    WEBInfantile 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 ...

    DA: 14 PA: 59 MOZ Rank: 18

  • Infantile neuroaxonal dystrophy: MedlinePlus Genetics

    medlineplus.gov

    https://medlineplus.gov/genetics/condition/infantile-neuroaxonal-dystrophy/

    WEBInfantile 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.

    DA: 90 PA: 13 MOZ Rank: 91

  • PLA2G6-Associated Neurodegeneration - Symptoms, Causes, …

    rarediseases.org

    https://rarediseases.org/rare-diseases/infantile-neuroaxonal-dystrophy/

    WEBJun 14, 2022 · Based on an individual’s age of onset and symptoms, their disease may be classified as one of three types of PLAN: infantile neuroaxonal dystrophy (INAD), a juvenile onset form called atypical neuroaxonal dystrophy (aNAD) or an adult-onset type called PLA2G6-related dystonia-parkinsonism.

    DA: 30 PA: 86 MOZ Rank: 11


  • Infantile Neuroaxonal Dystrophy - BrainFacts

    brainfacts.org

    https://www.brainfacts.org/Diseases-and-Disorders/Neurological-Disorders-AZ/Diseases-A-to-Z-from-NINDS/Infantile-Neuroaxonal-Dystrophy

    WEBInfantile 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.

    DA: 55 PA: 23 MOZ Rank: 36

  • Infantile neuroaxonal dystrophy - About the Disease - Genetic …

    nih.gov

    https://rarediseases.info.nih.gov/diseases/3957/infantile-neuroaxonal-dystrophy/

    WEBSummary. Infantile neuroaxonal dystrophy is a type of lipid storage disorder that mostly affects the nervous system. It has two forms, a classic form and an atypical form. Infantile neuroaxonal dystrophy is caused by changes (pathogenic variants) in the PLA2G6 gene and is inherited in an autosomal recessive pattern.

    DA: 37 PA: 13 MOZ Rank: 14

  • Infantile Neuroaxonal Dystrophy: Diagnosis and Possible …

    nih.gov

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295457/

    WEBDec 10, 2018 · Infantile neuroaxonal dystrophy (INAD) is a neurodegenerative disorder related to mutations in the PLA2G6 gene. Various mutations of PLA2G6 lead to dysfunctional A2 phospholipase that leads to mitochondrial and axonal membrane defects. These defects cause neuronal damage visualized as axonal swellings and accumulation …

    DA: 80 PA: 35 MOZ Rank: 76

  • The natural history of infantile neuroaxonal dystrophy - PMC

    nih.gov

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193406/

    WEBMay 1, 2020 · Infantile neuroaxonal dystrophy (INAD) is a rapidly progressive neurodegenerative disorder of early onset causing premature death. It results from biallelic pathogenic variants in PLA2G6, which encodes a calcium-independent phospholipase A2. …

    DA: 13 PA: 70 MOZ Rank: 5

  • Infantile neuroaxonal dystrophy - MedlinePlus

    medlineplus.gov

    https://medlineplus.gov/download/genetics/condition/infantile-neuroaxonal-dystrophy.pdf

    WEBInfantile 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.

    DA: 11 PA: 32 MOZ Rank: 88