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1.
J Postgrad Med ; 2000 Apr-Jun; 46(2): 91-3
Artículo en Inglés | IMSEAR | ID: sea-116731

RESUMEN

Scleredema adultorum is a rare connective tissue disorder reported usually following streptococcal infection, influenza, measles, and mumps. It has been reported occasionally following trauma and tuberculous lymphadenitis. This is a report of scleredema adultorum developing after chicken pox in an eight-year-old male child. The diagnosis was established by characteristic picture on skin biopsy using special stain. The patient had a benign course and a spontaneous recovery in two weeks. The case has been reported as the first case of scleredema adultorum developing after chicken pox.


Asunto(s)
Varicela/complicaciones , Niño , Humanos , Masculino , Escleredema del Adulto/diagnóstico
3.
J Postgrad Med ; 1995 Jan-Mar; 41(1): 21-2
Artículo en Inglés | IMSEAR | ID: sea-117210

RESUMEN

A neonate was born to a mother who had consumed an organophosphorus(OPC) compound with suicidal intent. The mother was administered atropine and this caused mydriasis in the neonate without any other pharmacological effects. There was no evidence of placental dysfunction. There are no case reports of OPC consumed in pregnancy and its effect on neonates or of effects of massive doses of atropine in the mother and its effects on the fetus or the newborn.


Asunto(s)
Atropina/administración & dosificación , Femenino , Humanos , Recién Nacido , Insecticidas/envenenamiento , Masculino , Intercambio Materno-Fetal , Midriasis/inducido químicamente , Compuestos Organofosforados , Embarazo , Complicaciones del Embarazo , Efectos Tardíos de la Exposición Prenatal , Intento de Suicidio
5.
Indian Pediatr ; 1994 Nov; 31(11): 1351-5
Artículo en Inglés | IMSEAR | ID: sea-6964

RESUMEN

The jejunal disaccharidases, sucrase, maltase and lactase, were determined in jejunal biopsies obtained from 43 malnourished children and 10 controls. In the study group, 63% were girls and 93% had severe malnutrition. Lactase activity was significantly reduced in third and fourth degree malnutrition (p < 0.05 and p < 0.005, respectively), but maltase activity was significantly reduced only in the fourth degree malnutrition (p < 0.01). After recovery, maltase and sucrase activities showed a marginally significant increase (p = 0.06), where lactase showed no significant increase (p > 0.05). We conclude that jejunal disaccharidase activity decreases significantly with increasing severity of malnutrition, lactase being the most severely affected and the last to recover.


Asunto(s)
Biopsia , Estudios de Casos y Controles , Niño , Trastornos de la Nutrición del Niño/enzimología , Preescolar , Femenino , Humanos , Lactante , Yeyuno/enzimología , Masculino , Desnutrición Proteico-Calórica/enzimología , Sacarasa/metabolismo , alfa-Glucosidasas/metabolismo , beta-Galactosidasa/metabolismo
6.
J Postgrad Med ; 1994 Jan-Mar; 40(1): 18-20
Artículo en Inglés | IMSEAR | ID: sea-115573

RESUMEN

Blood culture reports were studied in 1266 cases of clinically suspected neonatal septicemia, to determine the bacteriological profile and antibiotic sensitivity pattern of the cultured isolates. Blood culture was positive in 24.88% of cases. Gram negative septicemia was encountered in 87.1% of these neonates. Klebsiella and Enterobacter species were the predominant pathogens amongst Gram negative organisms. Of Gram positive isolates, Staphylococcus aureus was the predominant isolate (79.0%). Salmonella species was isolated in 2.4% of these cases.


Asunto(s)
Antibacterianos/farmacología , Bacteriemia/microbiología , Bacterias/efectos de los fármacos , Farmacorresistencia Microbiana , Humanos , Recién Nacido , Factores de Tiempo
7.
Indian J Pediatr ; 1993 Nov-Dec; 60(6): 813-8
Artículo en Inglés | IMSEAR | ID: sea-84010

RESUMEN

Spondylocostal dysostosis is a rare condition characterized by short stature due to a short trunk, multiple morphological abnormalities of the vertebrae and ribs due to malsegmentation of the axial skeleton. Radiological features include reduced number of vertebrae and ribs, hemivertebrae, fused or sagitally cleft vertebrae or multiple rib fusions. Three distinct clinical entities are described. We report nine cases of this syndrome, seven were infants and presented with an abnormal shape of the thorax. Two of them had a meningocoele, and one succumbed to the CNS anomalies on the third day of life. The other two cases were two and eight years of age. Cardiac lesion was detected in one case and renal malformations in three cases. Reduction in the rib number was present in all cases, and rib fusion in seven cases. Thoracic vertebral dysegmentation was noted in all, lumbar in three and cervical in one case. This is the first large series from India. No clear single etiology was established.


Asunto(s)
Anomalías Múltiples/genética , Enfermedades del Desarrollo Óseo/genética , Niño , Preescolar , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Costillas/anomalías , Columna Vertebral/anomalías , Síndrome
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