आईएसएसएन: 2572-4983

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खुला एक्सेस

हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।

ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं

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अमूर्त

Clinical profile of Acute Pancreatitis in children and adolescents from a single Centre in Northern India.

Nida mirza

Purpose: There has been an increase incidence of pancreatitis in children over the world, studies in developed countries shows increasing childhood obesity leading to increase in biliary disorders is cause for increasing incidence of pancreatitis in children, however there is sparse data from the developing countries. This study was undertaken to determine the characteristics of Indian children with acute pancreatitis mainly the clinical features, etiology, complication, association, genetic factors and outcome and recurrence. Methods: We performed a retrospective study of all patients under the age of 18 years who had a final diagnosis of pancreatitis admitted at our centre between 2017 and 2019. Results: During the 3-year period from 2017 to 2019, 40 patients (males-62.5%) were admitted at our centre with acute pancreatitis. We found a definite etiology in most cases (n= 25, 62.5%) of patients which were broadly grouped into 7 etiologies: Structural, Genetic, Drug induced, Systemic disease/underlying illness,
Cholelithiasis-related, Metabolic and Autoimmune. Recurrence of acute episodes were noted in 13 patients (32.5%). Of these, 11 were found to have a genetic mutation, underlying structural abnormality or systemic illness. Conclusions: we found that most cases of pancreatitis in children were of mild severity and the etiology were quite different than adults and most cases of acute recurrent pancreatitis have a definite etiology of either genetic mutation or structural anomaly.

अस्वीकृति: इस सारांश का अनुवाद कृत्रिम बुद्धिमत्ता उपकरणों का उपयोग करके किया गया है और इसे अभी तक समीक्षा या सत्यापित नहीं किया गया है।