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1.
Indian Pediatr ; 2018 Oct; 55(10): 880-882
Article | IMSEAR | ID: sea-199187

Résumé

Objective: To study the bone mineral content and density in children with congenital adrenalhyperplasia (CAH). Methods: 35 children with congenital adrenal hyperplasia and 35 healthycontrols. Bone mineral content and density were studied by Dual Energy X-rayabsorptiometry. Results: The mean (SD) of lumbar spine bone mineral density (g/cm2) [0.590(0.100) vs 0.589 (0.088) (P=0.97)], total Body less head bone mineral density (g/cm2) [0.536(0.090) vs 0.548 (0.111) (P=0.64)], lumbar spine bone mineral content (g) [29.85 (27.63) vs31.03 (29.19) (P=0.86)], and total body less head bone mineral content (g) [254.27 (281.25)vs 273.07 (330.71) (P=0.79)] were not different between children with CAH and controls,respectively. Conclusion: Bone mineral density and content in children with congenitaladrenal hyperplasia are maintained in the normal range.

4.
Indian J Pediatr ; 2009 Mar; 76(3): 313-4
Article Dans Anglais | IMSEAR | ID: sea-79863

Résumé

Thiamine responsive megaloblastic anemia syndrome (TRMA) is a clinical triad characterized by thiamine-responsive anemia, diabetes mellitus and sensorineural deafness. We report a 4-year-old girl with TRMA whose anemia improved following administration of thiamine and this case report sensitizes the early diagnosis and treatment with thiamine in children presenting with anemia, diabetes and deafness.


Sujets)
Anémie mégaloblastique/complications , Anémie mégaloblastique/diagnostic , Anémie mégaloblastique/traitement médicamenteux , Anémie mégaloblastique/génétique , Glycémie/métabolisme , Enfant d'âge préscolaire , Diabète de type 1/complications , Diabète de type 1/génétique , Femelle , Études de suivi , Surdité neurosensorielle/complications , Surdité neurosensorielle/génétique , Humains , Syndrome , Thiamine/usage thérapeutique
5.
Article Dans Anglais | IMSEAR | ID: sea-139031

Résumé

Background. There is little information on the clinical profile and outcome of children with diabetic ketoacidosis in India. We analysed the data of children managed by us at a tertiary care hospital. Methods. We retrospectively analysed the case records of 21 children (13 boys and 8 girls) with diabetic ketoacidosis admitted to our hospital from January 2004 to August 2008. They were managed using a standard protocol including intravenous fluids and insulin infusion. Blood glucose, serum electrolytes, blood urea, arterial blood gases and urinary ketones were monitored at regular intervals. The outcomes were assessed. Results. The median age at presentation was 8 years and 17 children (80%) were detected to have diabetes mellitus at the time of presentation. Twelve children (57%) presented with severe diabetic ketoacidosis. Polyuria with polydipsia was the commonest clinical presentation (17). All of them had elevated HbA1C levels. The average length of stay in the paediatric intensive care unit was 2.9 days. The median time for the arterial blood gases to become normal was 19 hours and for urinary ketones to become non-detectable was 28 hours. None of the children received bicarbonate and there were no complications or mortality. All the children were doing well on follow up at 3 months. Conclusion. The outcome of active management of diabetic ketoacidosis in children is rewarding. The use of a standard protocol for management was associated with no complications or mortality in our series.


Sujets)
Adolescent , Glycémie , Enfant , Enfant d'âge préscolaire , Diabète , Acidocétose diabétique/traitement médicamenteux , Électrolytes/sang , Femelle , Hémoglobine glyquée , Humains , Hypertension artérielle , Cétones/urine , Mâle , Études rétrospectives , Résultat thérapeutique
7.
Indian Pediatr ; 2008 Aug; 45(8): 697-9
Article Dans Anglais | IMSEAR | ID: sea-14410

Résumé

Scarabiasis is a condition where beetles temporarily infest the digestive tract and the scarabes are identified in the fly away from the anus at the time of the defecation. This article highlights this rare problem of scarabiasis in a 4 year old girl that responded to bowel cleansing and personal hygienic measures.


Sujets)
Canal anal , Animaux , Antiprotozoaires/usage thérapeutique , Coléoptères , Enfant d'âge préscolaire , Défécation , Ectoparasitoses/diagnostic , Femelle , Humains , Métronidazole/usage thérapeutique , Rectum
8.
Indian J Pediatr ; 2006 Feb; 73(2): 161-2
Article Dans Anglais | IMSEAR | ID: sea-81531

Résumé

Richner Hanhart syndrome is a rare inherited disorder involving the metabolism of tyrosine, a semi-essential amino acid and it should be considered in the differential diagnosis of a child presenting with ocular and skin lesions. We report a case of Richner Hanhart syndrome in a 19-month-old child, who presented with ocular and skin lesions.


Sujets)
Maladies de l'oeil/étiologie , Femelle , Humains , Nourrisson , Maladies de la peau/étiologie , Tyrosinémies/complications
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