Vitamin deficiencies in children: Lessons from clinical and neuroimaging findings

被引:4
作者
Dupuy, Gabrielle [1 ,2 ,8 ]
Roux, Charles-Joris [3 ]
Barrois, Remi [1 ,5 ]
Imbard, Apolline [4 ]
Pontoizeau, Clement [4 ]
Dangles, Marie Therese [1 ]
Aubart, Melodie [1 ]
Arnoux, Jean -Baptiste [2 ]
Margoses, Diane [2 ]
Brassier, Anais [2 ]
Marbach, Clothilde [2 ]
Berat, Claire -Marine [2 ]
Sarda, Eugenie [1 ]
Gitiaux, Cyril [1 ,5 ]
de Lonlay, Pascale [2 ,6 ]
Boddaert, Nathalie [3 ,7 ]
Schiff, Manuel [2 ,7 ]
Desguerre, Isabelle [1 ]
机构
[1] Univ Paris Cite, Necker Enfants Malades Hosp, AP HP, Pediat Neurol Dept, Paris, France
[2] Univ Paris Cite, Necker Enfants Malades Hosp, AP HP, Reference Ctr Inborn Errors Metab,Dept Pediat,G2M, Paris, France
[3] Univ Paris Cite, Necker Enfants Malades Hosp, AP HP, Pediat Radiol Dept, Paris, France
[4] Univ Paris Saclay, Necker Enfants Malades Hosp, AP HP, Dept Biochem, Paris, France
[5] Univ Paris Cite, Necker Enfants Malades Hosp, AP HP, Pediat Neurophysiol Dept, Paris, France
[6] Inst Necker Enfants Malades INEM, INSERM U1151, Paris, France
[7] Imagine Inst, INSERM UMRS 1163, Paris, France
[8] Hop Necker Enfants Malad, 149 Rue Sevres, F-75015 Paris, France
关键词
Wernicke encephalopathy; Vitamin deficiencies; Combined sclerosis of the spinal cord; Early onset encephalopathy; Scurvy; Child(ren); MAGNETIC-RESONANCE IMAGES; THIAMINE-DEFICIENCY; WERNICKES ENCEPHALOPATHY; BIOTINIDASE DEFICIENCY; MR FINDINGS; DIAGNOSIS; INFANTS;
D O I
10.1016/j.ejpn.2024.02.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and aims: 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. Methods: 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. Results: 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). Conclusions: 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.
引用
收藏
页码:6 / 15
页数:10
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