Basal nuclei lesions and cholecystitis as initial findings of late infantile metachromatic leukodystrophy
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),General Medicine,Surgery
Reference13 articles.
1. Gomez-Ospina N. Arylsulfatase A Deficiency. GeneReviews, 2006 May 30 [updated 2020 Apr 30].
2. Acute-onset paralytic strabismus in toddlers is important to consider as a potential early sign of late-infantile Metachromatic Leukodystrophy;Beerepoot;Eur. J. Paediatr. Neurol.,2022
3. Peripheral neuropathy as the sole initial finding in three children with infantile metachromatic leukodystrophy;Haberlandt;Eur. J. Paediatr. Neurol.,2009
4. Subacute demyelinating peripheral neuropathy as a novel presentation of late infantile metachromatic leukodystrophy;Gonorazky;Muscle Nerve,2017
5. A homozygote for the c.459+1G>A mutation in the ARSA gene presents with cerebellar ataxia as the only first clinical sign of metachromatic leukodystrophy;Lugowska;J. Neurol. Sci.,2014
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