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Infantile Tremor Syndrome

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dc.contributor.author Robin Mukkath Thomas, Raghavendra H Gobbur
dc.date.accessioned 2019-11-06T12:29:12Z
dc.date.available 2019-11-06T12:29:12Z
dc.date.issued 2016
dc.identifier.issn 00196061
dc.identifier.uri http://hdl.handle.net/123456789/1166
dc.description.abstract Child was unable to cry and feed. He was exclusively breast fed. He was classified as grade 2 (IAP) malnutrition; he also had hyperpigmentation over limbs, pallor and hepatosplenomegaly. Tremors were absent during sleep, and got aggravated during activities (Web Video 1). His hemoglobin was 5.8 g/dL with dimorphic blood picture. EEG was normal and MRI showed diffuse cerebral atrophy. Mother’s serum B12 levels were low (<200 pg/mL) but child’s serum B12 levels were normal, probably because of prior treatment with injectable B12. A diagnosis of Infantile tremor syndrome (ITS) was made. Child received WHO protocol of management for moderate malnutrition. The child received blood transfusion, vitamin (A, D, B complex and C) and mineral (zinc, magnesium, calcium) supplementation. Propranolol (0.5 mg/kg/day) was started, and increased to 2 mg/kg/day till the tremor decreased in intensity and general condition of child improved. Kahn’s nutritional recovery syndrome, infections (viral encephalitis/encephalopathy), phenothiazine toxicity, degenerative diseases, and enzyme defects in tyrosine metabolism leading to substantia nigra depigmentation are the differential diagnoses of ITS. en_US
dc.language.iso en en_US
dc.publisher BLDE(Deemed to be University) en_US
dc.subject A previously normal, 15monthold boy, born at term to nonconsanguineous parents, was hospitalized for generalized tremors for 3 days. en_US
dc.title Infantile Tremor Syndrome en_US
dc.type Article en_US


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