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1.
Indian Pediatr ; 61(7): 649-655, 2024 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-38803097

RESUMEN

OBJECTIVES: To compare the urinary bisphenol A (BPA) levels in bottle-fed and never bottle-fed infants and under-five children and to determine the impact of bottle-feeding practices and sociodemographic factors on urinary BPA levels. METHODS: A community-based cross-sectional study was carried out on children aged between 2 to 60 months attending the Anganwadi centres in Chandigarh. RESULTS: Urine samples were collected from 184 children, out of which 94.56% (n = 174) children had detectable urinary BPA levels. The mean (SD) BPA level was 2.74 (2.60) ng/ml and BPA was detected in 93.9% of 'ever' bottle-fed children (n = 93/99) and 95.3% of 'never' bottle-fed children (n = 81/85) (P = 0.69). On multivariate regression analysis, there were no significant predictors for high (≥ 75th percentile) urinary BPA levels. Still, the odds of urinary BPA levels ≥75th percentile showed higher trend for significance among children from middle/higher socioeconomic background in reference to lower socioeconomic stratum (adjusted OR 7.02; 95% CI 1.24, 133.25; P = 0.07) and among children whose feeding bottles were brushed once or twice daily in reference to group with no daily brushing (adjusted OR 3.92, 95% CI 0.95, 20.56; P = 0.07). CONCLUSIONS: Although feeding with plastic bottle did not emerge as a statistically significant risk factor for BPA exposure, yet detection of BPA levels among majority of study children signals urgent need for unmasking exposure to other sources given the potential long-term toxicity of BPA among infants and young children.


Asunto(s)
Compuestos de Bencidrilo , Alimentación con Biberón , Fenoles , Humanos , Compuestos de Bencidrilo/orina , Fenoles/orina , Lactante , India , Alimentación con Biberón/estadística & datos numéricos , Preescolar , Femenino , Masculino , Estudios Transversales , Monitoreo Biológico/métodos
2.
Am J Med Genet A ; 185(5): 1550-1553, 2021 05.
Artículo en Inglés | MEDLINE | ID: mdl-33615695

RESUMEN

Frontometaphyseal dysplasia (FMD) is a rare genetic disorder with morphological abnormalities of the skeletal and extra skeletal tissues. It belongs to the group of otopalatodigital spectrum disorders. Here we report a 12-year-old boy from India with features of frontometaphyseal dysplasia who had severe scoliosis with neurological complications due to spinal cord compromise. Clinical examination of his mother also revealed mild features of FMD. The manuscript highlights the clinical presentation of the disorder and discusses the clinical heterogeneity of the otopalatodigital spectrum disorders.


Asunto(s)
Anomalías Múltiples/genética , Frente/anomalías , Enfermedades Genéticas Ligadas al Cromosoma X/genética , Osteocondrodisplasias/genética , Escoliosis/genética , Anomalías Múltiples/fisiopatología , Niño , Frente/diagnóstico por imagen , Frente/fisiopatología , Genes Ligados a X/genética , Enfermedades Genéticas Ligadas al Cromosoma X/diagnóstico por imagen , Enfermedades Genéticas Ligadas al Cromosoma X/fisiopatología , Humanos , India/epidemiología , Masculino , Madres , Mutación/genética , Osteocondrodisplasias/diagnóstico por imagen , Osteocondrodisplasias/fisiopatología , Fenotipo , Escoliosis/complicaciones , Escoliosis/diagnóstico , Escoliosis/fisiopatología , Médula Espinal/patología
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