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Medical condition
Infantile neuroaxonal dystrophy
Other names
INAD, Seitelberger disease
Infantile neuroaxonal dystrophy has an autosomal recessive pattern of inheritance.
Specialty
Neurology
Usual onset
Six months to two year of age
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, such as crawling or beginning to speak. Eventually they lose previously acquired skills.
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Infantileneuroaxonaldystrophy (INAD) is a rare pervasive developmental disorder that primarily affects the nervous system. Individuals with infantile...
clinical study began in 2019. An open-label clinical study for infantileneuroaxonaldystrophy evaluating long-term evaluation of efficacy, safety, tolerability...
and sensorimotor impairment. The most severe form is called infantileneuroaxonaldystrophy (INAD), also Neurodegeneration with brain iron accumulation...
clinical study began in 2019. An open-label clinical study for infantileneuroaxonaldystrophy evaluating long-term evaluation of efficacy, safety, tolerability...
tolerability, and pharmacokinetics of RT001 in the treatment of infantileneuroaxonaldystrophy started in the Summer 2018. After a petition for access filed...
critical role in improving the outcome of individuals with PDD. Infantileneuroaxonaldystrophy Multiple complex developmental disorder Multisystem developmental...
bees, blennies and viper snakes. Patatin-like phospholipase Infantileneuroaxonaldystrophy "phospholipase" at Dorland's Medical Dictionary Molinari, Giuliano;...
in the alpha-N-acetylgalactosaminidase gene that causes an infantileneuroaxonaldystrophy". J. Clin. Invest. 86 (5): 1752–6. doi:10.1172/JCI114901. PMC 296929...
developed by Retrotope, is in a compassionate use trial in infantileneuroaxonaldystrophy and has successfully completed a Phase I/II trial in Friedreich's...
against further use of the Reiter eponym." Seitelberger disease Infantileneuroaxonaldystrophy Franz Seitelberger [de] "Franz Seitelberger, a Vienna neurologist...
neurodegenerative diseases such as Friedreich’s ataxia and infantileneuroaxonaldystrophy. FDA has granted it an orphan drug designation and it passed...
Microphthalmia / anophthalmia (non-syndromic) caused by CHX10 mutation Infantileneuroaxonaldystrophy: demonstrating that it is a storage disease caused by a mutation...
Atwal, P.; Milner, P.; Shchepinov, M. S. (2020). "Treatment of infantileneuroaxonaldystrophy with RT001: A di‐deuterated ethyl ester of linoleic acid: Report...
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