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2.
Indian J Pediatr ; 89(10): 983-988, 2022 10.
Artigo em Inglês | MEDLINE | ID: mdl-34480715

RESUMO

OBJECTIVE: To determine the prevalence of short stature, delayed puberty, hypothyroidism, and diabetes mellitus in multiply transfused patients of beta thalassemia major and their correlation with serum ferritin. METHODS: A descriptive observational study was conducted in a tertiary care center in Indore, Madhya Pradesh from 2014 to 2016. All children with thalassemia major of the age group 8 to 18 y attending outpatient department or admitted in ward were included in the study. Detailed clinical history, demographic data, compliance to transfusion and chelation therapy, and growth parameters were recorded. Blood samples to look for endocrinopathies and serum ferritin were assessed. Tanner staging was done to assess for delayed puberty. RESULTS: Mean age of study participants (n = 50) was 15.98 ± 3.4 y. Short stature (n = 44; 88%), delayed puberty (n = 33; 71.7%), hypothyroidism (n = 6; 16%), and diabetes mellitus (n = 5; 10%) were the endocrinal abnormalities found. Mean serum ferritin level was 3122 ± 2117 ng/mL. Serum ferritin had significant positive correlation with serum TSH (thyroid stimulating hormone), fasting blood sugars, postprandial blood sugar, and delayed puberty. CONCLUSION: Evaluation of endocrinopatines must be carried out in thalassemia major patients regularly by pediatricians to detect and treat endocrinal complications. Importance of chelation therapy must be emphasized frequently to parents and patients.


Assuntos
Diabetes Mellitus , Hipotireoidismo , Puberdade Tardia , Talassemia beta , Adolescente , Glicemia , Criança , Ferritinas , Humanos , Hipotireoidismo/epidemiologia , Hipotireoidismo/etiologia , Índia/epidemiologia , Puberdade Tardia/complicações , Tireotropina , Talassemia beta/complicações , Talassemia beta/epidemiologia , Talassemia beta/terapia
3.
Indian Pediatr ; 52(5): 443-4, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-26061944
4.
Indian Pediatr ; 52(2): 152-4, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25691189

RESUMO

BACKGROUND: Recurrent Kawasaki disease is rare. CASE CHARACTERISTICS: An eight-month old infant had classic Kawasaki disease with transient coronary artery dilatation. OBSERVATIONS: Recurrence of incomplete Kawasaki disease after two years of initial diagnosis. OUTCOME: The index episode of Kawasaki disease was resistant to single infusion of immunoglobulin, while repeat episode responded within 24 hours of institution of therapy. MESSAGE: Early recognition of recurrent Kawasaki disease requires a high index of suspicion.


Assuntos
Síndrome de Linfonodos Mucocutâneos , Pré-Escolar , Pé/patologia , Humanos , Lactente , Masculino , Recidiva , Pele/patologia , Resultado do Tratamento
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