Limb torsion and developmental regression for one month after hand, foot and mouth disease in an infant / 中国当代儿科杂志
Zhongguo dangdai erke zazhi
; Zhongguo dangdai erke zazhi;(12): 426-430, 2016.
Article
en Zh
| WPRIM
| ID: wpr-261215
Biblioteca responsable:
WPRO
ABSTRACT
A one-year-old girl visited the hospital due to limb torsion and developmental regression for one month after hand, foot and mouth disease. At the age of 11 months, she visited a local hospital due to fever for 5 days and skin rash with frequent convulsions for 2 days and was diagnosed with severe hand, foot and mouth disease, viral encephalitis, and status epilepticus. Brain MRI revealed symmetric abnormal signals in the bilateral basal ganglia, bilateral thalamus, cerebral peduncle, bilateral cortex, and hippocampus. She was given immunoglobulin, antiviral drugs, and anticonvulsant drugs for 2 weeks, and the effect was poor. Blood and urine screening for inherited metabolic diseases were performed to clarify the etiology. The analysis of urine organic acids showed significant increases in glutaric acid and 3-hydroxyglutaric acid, which suggested glutaric aciduria type 1, but her blood glutarylcarnitine was normal, and free carnitine significantly decreased. After the treatment with low-lysine diets, L-carnitine, and baclofen for 1 month, the patient showed a significant improvement in symptoms. Hand, foot and mouth disease is a common viral infectious disease in children, and children with underlying diseases such as inherited metabolic diseases and immunodeficiency may experience serious complications. For children with hand, foot and mouth disease and unexplained encephalopathy, inherited metabolic diseases should be considered.
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Índice:
WPRIM
Asunto principal:
Anomalía Torsional
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Encefalopatías Metabólicas
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Discapacidades del Desarrollo
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Glutaril-CoA Deshidrogenasa
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Errores Innatos del Metabolismo de los Aminoácidos
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Enfermedad de Boca, Mano y Pie
Límite:
Female
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Humans
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Infant
Idioma:
Zh
Revista:
Zhongguo dangdai erke zazhi
Año:
2016
Tipo del documento:
Article