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Infantile Tremor Syndrome Persistence in Era of Development: An Old Story
Anand Kumar1, Gayathri M Rao1, Beena V Shetty1
1Department of Biochemistry, Center for Basic Sciences, Kasturba Medical College, Bejai, Mangalore, Karnataka 575004 India.
Insights
Infantile tremor syndrome (ITS) persists despite malnutrition programs. This case highlights severe ITS with neurological and hematological issues in a young child.
Area of Science:
- Pediatrics
- Neurology
- Hematology
Background:
- Infantile tremor syndrome (ITS) is prevalent globally, particularly in developing nations.
- Despite ongoing protein-energy malnutrition awareness programs, ITS persists, indicating a need for further research and intervention.
Observation:
- A 13-month-old female presented with respiratory distress, fever, limb tremors, and loss of developmental milestones.
- Clinical examination revealed pallor and hyperpigmentation in the axilla and toes.
Findings:
- Investigative findings included megaloblastic erythroid hyperplasia and severe anemia (hemoglobin 1.6 g%).
- Brain CT scan demonstrated central atrophic changes, suggesting neurological involvement.
Implications:
- This case underscores the critical need for early diagnosis and comprehensive management of ITS.
- Highlighting the neurological and hematological complications of ITS is crucial for improving patient outcomes and public health strategies.
Abstract:
Infantile tremor syndrome is seen worldwide more commonly in the developing countries. Although various protein energy malnutrition awareness programme being run in many of these countries including India yet there is persistence of this disease. Here we present a case of 13 month old female child who visited RAPCC paediatrics OPD of Govt. Wenlock Hospital Mangaluru with history of respiratory distress, fever, tremor in limbs and loss of milestones. On examination she had pallor, hyper pigmentation in axilla and toes. Investigatory findings showed megaloblastic erythroid hyperplasia, hemoglobin- 1.6 g % and CT scan of brain showed central atrophic changes.
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