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Vitamin deficiencies in children: Lessons from clinical and neuroimaging findings.

Authors :
Dupuy, Gabrielle
Roux, Charles-Joris
Barrois, Rémi
Imbard, Apolline
Pontoizeau, Clément
Dangles, Marie Thérèse
Aubart, Mélodie
Arnoux, Jean-Baptiste
Margoses, Diane
Brassier, Anaïs
Marbach, Clothilde
Bérat, Claire-Marine
Sarda, Eugénie
Gitiaux, Cyril
de Lonlay, Pascale
Boddaert, Nathalie
Schiff, Manuel
Desguerre, Isabelle
Source :
European Journal of Paediatric Neurology; May2024, Vol. 50, p6-15, 10p
Publication Year :
2024

Abstract

Water-soluble vitamins play an essential coenzyme role in the nervous system. Acquired vitamin deficiencies are easily treatable, however, without treatment, they can lead to irreversible complications. This study aimed to provide clinical, laboratory parameters and neuroimaging data on vitamin deficiencies in an attempt to facilitate early diagnosis and prompt supplementation. From July 1998 to July 2023, patients at Necker-Enfants-Malades Hospital presenting with acute neurological symptoms attributed to acquired vitamin deficiency were included. Clinical data were extracted from Dr Warehouse database. Neuroimaging, biochemical and electrophysiological data were reviewed. Patients with vitamin B1 deficiency exhibited abnormal eye movements (n = 4/4), fluctuations in consciousness (n = 3/4), and ataxia (n = 3/4). Brain MRI showed alterations of fourth ventricle region (n = 4/4), periaqueductal region (n = 4/4), tectum (n = 3/4), and median thalami (n = 3/4). Patients with vitamin B2 deficiency presented with early onset hypotonia (n = 3/4), hyperlactatemia (n = 4/4), and hyperammonemia (n = 4/4). Plasma acylcarnitines revealed a multiple acyl-coA dehydrogenase deficiency-like profile (n = 4/4). In vitamin B12 deficiency, young children presented with developmental delay (n = 7/7) and older children with proprioceptive ataxia (n = 3/3). Brain MRI revealed atrophy (n = 7/7) and spinal MRI hyperintensity in posterior cervical columns (n = 3/3). Metabolic findings showed elevated methylmalonic acid (n = 6/7) and hyperhomocysteinemia (n = 6/7). Patients with vitamin C deficiency exhibited gait disturbances and muscle weakness (n = 2/2). Acquired vitamin deficiencies may display reversible clinical symptoms mimicking inherited metabolic disorders. Some situations raise suspicion for diagnosis: concordant clinical presentation, suggestive neuroimaging findings, and/or biochemical evidence. Any acute neurological condition should be treated without waiting for definitive biochemical confirmation. • Although they are not extensively documented, vitamin deficiencies do occur in children. • Acquired vitamin deficiencies are easily treatable but without treatment, can lead to irreversible neurological complications. • One should consider a vitamin deficiency in the presence of unexplained neurological symptoms. • One should consider a vitamin deficiency in an exclusively breastfed infant showing signs of developmental stagnation. • Initiation vitamin supplementation should not be delayed pending conclusive biochemical confirmation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10903798
Volume :
50
Database :
Supplemental Index
Journal :
European Journal of Paediatric Neurology
Publication Type :
Academic Journal
Accession number :
177906644
Full Text :
https://doi.org/10.1016/j.ejpn.2024.02.013