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1.
Journal of the Korean Society of Neonatology ; : 32-41, 2005.
Artigo em Coreano | WPRIM | ID: wpr-85841

RESUMO

PURPOSE: A prospective, controlled trial was conducted to evaluate growth, bone mineralization, and nutritional status receiving preterm human milk supplemented with a newly formulated Maeil human milk fortifier. METHODS: Twenty five fortified human milk-fed and preterm formula-fed infants with a birth weight < 1, 800 g and gestational age <35 weeks, who were born at Ajou University Hospital from March, 2003 through August, 2004 were studied. Growth, biochemical indices of bone mineralization, feeding tolerance, morbidity and wrist X-ray were assessed serially. Total body bone mineral density was measured by dual energy X-ray absorptiometry at 2 and 5months of age. RESULTS: There were no differences in growth, including weight, height and head circumference, between two groups. Serum Ca, P, ALP and other biochemical indices were similar. Although low grade rickets (grade I and II) were occasionally found on wrist X-ray, the rate of occurrence and severity were similar. The bone mineral densities of both group showed no difference. CONCLUSION: The fortified human milk-fed infants and preterm formula-fed infants showed no difference in growth, and bone mineralization. This newly formulated Maeil human milk fortifier can be safely used in preterm infants.


Assuntos
Humanos , Lactente , Recém-Nascido , Absorciometria de Fóton , Peso ao Nascer , Densidade Óssea , Calcificação Fisiológica , Idade Gestacional , Cabeça , Recém-Nascido Prematuro , Leite Humano , Estado Nutricional , Estudos Prospectivos , Raquitismo , Punho
2.
Journal of Korean Society of Pediatric Endocrinology ; : 168-172, 2004.
Artigo em Coreano | WPRIM | ID: wpr-222693

RESUMO

PURPOSE:Chronic autoimmune thyroiditis is the most common thyroid disease in children and adolescents, and also is the most common cause of hypothyroidism in children and adolescents. We studied the clinical manifestations and natural courses of chronic autoimmune thyroiditis in children and adolescents. METHODS:We analyzed retrospectively twenty one children and adolescents who were diagnosed as chronic autoimmune thyroiditis before 15 years of age. The diagnoses were made from July 1997 to February 2004 at Ajou Univesity Hospital. We reviewed the clinical manifestations and thyroid functions of these patients. RESULTS:Nineteen patients were female and two were male. The mean age at diagnosis was 9.95+/-3.1 years, the mean duration of follow up was 23.52+/-22.98 months. At diagnosis, the most common chief complaint was goiter (15 patients/21 patients) and the others were short stature, easy fatigue, cardiac murmur and weight loss. Eighteen patients had goiters at diagnosis. Four had familial history of thyroid disease, Three of them had maternal history of thyroid disease and one had paternal history of thyroid disease. At diagnosis, Seven patients were euthyroid and four patients were hyperthyroid, eighteen patients had antithyroglobulin antibody, seventeen patients had antimicrosomal antibody, fourteen patients had both of them. At last follow-up, eight patients were euthyroid and ten patients were hypothyroid, three patients were hyperthyroid. CONCLUSION: Chronic autoimmune thyroiditis in children and adolescents can have the various important influences on the metabolism including the growth. The clinical manifestations and thyroid functions should be monitored in children and adolescents with chronic autoimmune thyroiditis.


Assuntos
Adolescente , Criança , Feminino , Humanos , Masculino , Diagnóstico , Fadiga , Seguimentos , Bócio , Sopros Cardíacos , Hipotireoidismo , Metabolismo , Estudos Retrospectivos , Doenças da Glândula Tireoide , Glândula Tireoide , Tireoidite Autoimune , Redução de Peso
3.
Journal of the Korean Society of Pediatric Nephrology ; : 223-228, 2003.
Artigo em Coreano | WPRIM | ID: wpr-45536

RESUMO

Oligmeganephronia is congenital hypoplasia of kidney with renal pathology showing very small number of nephrons with compensatory hypertrophy of the remaining glomeruli. A 7- year-old girl was referred to our nephrology clinic due to hematuria detected on school screening urinalysis and diagnosed as chronic renal failure and oligomeganephronia on renal biopsy. We are reporting the clinical and histomorphometric changes for the four years follow-up with review of literatures.


Assuntos
Feminino , Humanos , Biópsia , Seguimentos , Hematúria , Hipertrofia , Rim , Falência Renal Crônica , Programas de Rastreamento , Nefrologia , Néfrons , Patologia , Urinálise
4.
Journal of the Korean Society of Pediatric Nephrology ; : 239-244, 2003.
Artigo em Coreano | WPRIM | ID: wpr-45533

RESUMO

99mTc-MAG3 Scintigraphic Scan is sensitive at depicting focal parenchymal abnormalities and can be used for the measurement of overall renal function. We experienced a 12-year-old girl presenting with fever and flank pain. On the ultrasonogram and post-voiding delayed image of 99mTc-MAG3 scintigraphic scan, severe right cortical atrophy and hydronephrosis with vesicoureteral reflux were detected. We could demonstrate the reflux nephropathy by these two diagnostic work-up without conventional voiding cystourethrography.


Assuntos
Criança , Feminino , Humanos , Atrofia , Febre , Dor no Flanco , Hidronefrose , Tecnécio Tc 99m Mertiatida , Ultrassonografia , Refluxo Vesicoureteral
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