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1.
Indian J Pediatr ; 2007 Aug; 74(8): 768-9
Artigo em Inglês | IMSEAR | ID: sea-80258

RESUMO

Innominate artery may cross the trachea and cause airway obstruction is a rare cause of vascular obstruction of airway. We describe a child with stridor, inability to extubate in whom the diagnosis was suspected on fluoroscopy and confirmed by angiography. Reimplantation of the innominate artery resulted in excellent results with longterm follow up. Variantions of this condition and modalities for confirmation of diagnosis are discussed.


Assuntos
Tronco Braquiocefálico/anormalidades , Angiografia Coronária , Diagnóstico Diferencial , Ecocardiografia , Eletrocardiografia , Fluoroscopia , Humanos , Lactente , Masculino , Radiografia Torácica , Estenose Traqueal/diagnóstico
2.
Indian J Pediatr ; 2005 Oct; 72(10): 835-7
Artigo em Inglês | IMSEAR | ID: sea-79336

RESUMO

OBJECTIVE: This study was carried out to detect the incidence of erythrocytic Glucose-6 -Phosphate dehydrogenase (G-6-PD) deficiency, to compare the incidence of hyperbilirubinemia in G-6-PD deficient neonates as compared to G-6-PD normal neonates and to asses the usefulness of neonatal screening for G-6-PD deficiency. METHOD: In a retrospective hospital based study 2,479 male and female neonates consecutively born at Indraprastha Apollo hospital between July 1998 to June 2003 who were screened for G-6-PD levels were evaluated for the incidence of G-6-PD deficiency. RESULTS: Incidence of G-6-PD deficiency was found to be 2.0%. Incidence in males was 283% and female was 1.05%. The incidence of hyperbilirubinemia was found to be 32% in G-6-PD deficient neonates which was significantly higher than the incidence of hyperbilirubinemia in neonates with normal G-6-PD, which was 12.3% (P< 0.001). CONCLUSION: Our data suggests that neonatal screening for G-6-PD deficiency is a useful test for preventing and early treatment of complications associated with it.


Assuntos
Fatores Etários , Bilirrubina/sangue , Estudos de Coortes , Feminino , Glucosefosfato Desidrogenase/sangue , Deficiência de Glucosefosfato Desidrogenase/complicações , Humanos , Hiperbilirrubinemia/diagnóstico , Índia/epidemiologia , Recém-Nascido , Masculino , Triagem Neonatal , Fototerapia , Mutação Puntual , Estudos Retrospectivos , Fatores Sexuais
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