Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/1166
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dc.contributor.authorRobin Mukkath Thomas, Raghavendra H Gobbur-
dc.date.accessioned2019-11-06T12:29:12Z-
dc.date.available2019-11-06T12:29:12Z-
dc.date.issued2016-
dc.identifier.issn00196061-
dc.identifier.urihttp://hdl.handle.net/123456789/1166-
dc.description.abstractChild 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.isoenen_US
dc.publisherBLDE(Deemed to be University)en_US
dc.subjectA previously normal, 15monthold boy, born at term to nonconsanguineous parents, was hospitalized for generalized tremors for 3 days.en_US
dc.titleInfantile Tremor Syndromeen_US
dc.typeArticleen_US
Appears in Collections:Faculty of Pediatrics

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