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1.
Indian Pediatr ; 2023 Jan; 60(1): 33-36
Article | IMSEAR | ID: sea-225403

ABSTRACT

Objective: To assess the growth and neurodevelopmental outcome of very low birth weight (VLBW) infants at corrected age of one year. Methods: This prospective cohort study enrolled VLBW infants delivered in a tertiary care hospital, and followed up till oneyear corrected age. The WHO Anthropo version 3.2.2 software was used to calculate weight for age, length for age, and head circumference z-score during follow up. Neurodevelopmental assessment was done using Developmental Assessment Scale for Indian Infants (DASII) at the age of one year. Results: The mean (SD) z-scores at one-year for weight for age, length for age and head circumference were -2.1 (1.1), -1.4 (1.03) and -2.2 (1.2), respectively. The mean (SD) DASII motor and mental scores were 90.8 (13.4) and 96.5 (13.2), respectively. Major and minor developmental abnormalities were noted in 9.4% and 18.2%, infants, respectively. Cerebral palsy was noted in 5.8% infants. Conclusion: VLBW infants showed impaired growth and significant developmental abnormalities at the corrected age of one year.

2.
Indian Pediatr ; 2018 Jul ; 55(7): 601-602
Article | IMSEAR | ID: sea-199116

ABSTRACT

Background: Schimmelpenning syndrome is a multisystem disorder. Casecharacteristics: A term female neonate with sebaceous nevi of the face had choroidosteoma of the right eye. Observation: At one month of age, the infant was observed tohave choroidal neovascularization that was successfully treated with laser photo-coagulation and anti-VEGF. Message: Choroid osteoma and neovascularization are rareassociations of Schimmelpenning syndrome, and should be screened for and managedearly.

3.
Indian Pediatr ; 2018 Apr; 55(4): 287-288
Article | IMSEAR | ID: sea-199057
4.
Article in English | IMSEAR | ID: sea-176344

ABSTRACT

Background & objectives: Genotyping has now become one of the major diagnostic means for almost all diseases. Among the advanced techniques that are used to study single nucleotide polymorphisms (SNPs), only a few are applicable for routine disease diagnosis. Their applicability mainly depends on three factors: cost, time, and accuracy. The primary objective of this study was to propose allele-specific real-time PCR as a rapid, low cost and simple genotyping method for routine diagnostics. Methods: Two SNPs, rs3014866 and rs2149356 were analysed using allele-specific real-time PCR. The polymerase chain reaction was carried out using RealQ PCR master mix containing SYBR Green DNA I dye followed by melt curve analysis. The results were validated by agarose gel electrophoresis and DNA sequencing. Results: The allelic discrimination and zygosity of the two SNPs were assessed by combined cycle threshold (Ct) and melting temperature (Tm) values. Variations in Ct and Tm values among the two alleles were observed in both rs3014866 (Ct: C allele - 24±1, T allele - 27±1; Tm: C allele - 82.5±0.3, T allele - 86.3±0.2) and rs2149356 (Ct: C allele - 24±1, A allele - 26±1; Tm: C allele - 79.4±0.2, A allele - 80.4±0.3). Based on the variations, homozygous and heterozygous alleles were detected. Agarose gel electrophoresis and DNA sequencing also confirmed the allelic variation and zygosity observed in real-time PCR. Interpretation & conclusions: In diagnostic settings where a large number of samples are analysed daily, allele-specific real-time PCR assay may serve as a simple, low cost and efficient method of genotyping

5.
Indian Pediatr ; 2015 May; 52(5): 382-383
Article in English | IMSEAR | ID: sea-171413
6.
Indian J Dermatol Venereol Leprol ; 2012 May-Jun; 78(3): 408-409
Article in English | IMSEAR | ID: sea-141113
7.
Indian J Pediatr ; 2010 May; 77(5): 515-517
Article in English | IMSEAR | ID: sea-142571

ABSTRACT

Objective. To study the serum levels of oxidative stress markers - malondialdehyde (MDA) and protein carbonyl in babies with perinatal asphyxia and to correlate their levels with the outcome in terms of mortality and neurodevelopmental sequelae. Methods. A group of 40 term AGA (appropriate for gestational age) infants with perinatal asphyxia were selected as cases and same number of healthy babies as controls. Serum levels of oxidative stress markers - malondialdehyde and protein carbonyl were determined in cord blood and at 48 hours of life. Their levels were correlated with the outcome of perinatal asphyxia in terms of mortality and the long term neurological outcome. Results. MDA and protein carbonyl, in cord blood were significantly higher among cases (5.88±1.40 μmol/L and 1.50±0.48 nmol/mg of protein respectively) than controls (3.11±0.82 μmol/L and 0.83±0.19 nmol/mg of protein respectively). Among the cases, MDA and protein carbonyl values at 48 hours of life (7.52 ± 1.06 μmol/L and 2.91 ± 0.62 nmol/mg of protein respectively) were significantly higher than those at birth. MDA at birth and 48 hours was significantly higher among babies who had seizures than those who remained seizure free. These values were also significantly higher in babies who expired as compared to those who survived. Protein carbonyl values though higher in those who had seizures and in those who expired, were not statistically significant from controls. MDA and protein carbonyl at birth and 48 hours were higher in babies with developmental delay but the association was not statistically significant. Conclusions. In hypoxic ischemic encephalopathy (HIE), oxidative stress markers MDA and protein carbonyl are high at birth and rise further at 48 hours and the values correlate with the morbidity and mortality. Therefore, determining the serum levels of oxidative stress markers MDA and protein carbonyl will be of benefit in predicting the outcome in perinatal asphyxia.


Subject(s)
Analysis of Variance , Asphyxia Neonatorum/blood , Biomarkers/blood , Case-Control Studies , Female , Fetal Blood , Gestational Age , Humans , Male , Infant, Newborn , Malondialdehyde/blood , Oxidative Stress , Prospective Studies , Protein Carbonylation , Statistics, Nonparametric
8.
Indian J Pediatr ; 2010 Apr; 77(4): 435-437
Article in English | IMSEAR | ID: sea-142554

ABSTRACT

Fulminant hepatic failure due to dengue infection is rare, although mild liver dysfunction is common. Here we report a fatal case of fulminant hepatitis in an infant infected with dengue 3 serotype. Attention must be given to the use of hepatotoxic drugs in some cases of dengue especially in infants.


Subject(s)
Dengue/complications , Humans , Infant , Liver Failure, Acute/etiology , Male , Shock, Septic/complications
9.
Indian J Dermatol Venereol Leprol ; 2010 Mar-Apr; 76(2): 220
Article in English | IMSEAR | ID: sea-140601
10.
Indian J Pediatr ; 2008 Dec; 75(12): 1223-5
Article in English | IMSEAR | ID: sea-82590

ABSTRACT

OBJECTIVE: To study the usefulness of cardiac enzymes in evaluating myocardial damage in perinatal asphyxia. METHODS: Thirty term babies with perinatal asphyxia and without any congenital malformations were selected as cases. They were compared with thirty healthy term babies without asphyxia. Myocardial dysfunction was evaluated using clinical, electrocardiography, echocardiography and cardiac enzymes i.e, troponin-T and CK-MB levels. RESULTS: Among the 30 cases 23 had evidence of myocardial involvement while one baby in the control group had ECG evidence compatible with cardiac involvement. Cardiac enzymes were significantly increased in babies with perinatal asphyxia. The mean level of C-troponin-T among cases and controls were 0.22+/-0.28 and 0.003+/-0.018 while CK-MB levels were 121+/-77.4 IU/L and 28.8 +/- 20.2 IU/L respectively. C-troponin-T had higher sensitivity and specificity compared to CK-MB levels. Moreover, C troponin-T levels correlated well with severity and outcome in babies with perinatal asphyxia. CONCLUSION: C-Tropopnin assay is useful in evaluating the severity of myocardial damage and outcome in perinatal asphyxia.


Subject(s)
Asphyxia Neonatorum/complications , Cardiomyopathies/diagnosis , Creatine Kinase, MB Form/blood , Humans , Infant, Newborn , Myocardium/enzymology , Prospective Studies , Sensitivity and Specificity , Troponin T/blood
11.
Indian J Pediatr ; 2007 Nov; 74(11): 1029-31
Article in English | IMSEAR | ID: sea-83282

ABSTRACT

Short rib polydactyly syndromes (SRPS) are a group of inherited autosomal recessive skeletal dysplasias. It is characterized by the triad of micromelia, polydactyly and short horizontal ribs with or without visceral involvement. We report a case of SRPS-2 in a fresh stillborn and discuss the differential diagnosis.


Subject(s)
Adult , Diagnosis, Differential , Female , Humans , Pregnancy , Short Rib-Polydactyly Syndrome/diagnosis , Stillbirth
12.
Indian J Pediatr ; 2007 Jul; 74(7): 623-5
Article in English | IMSEAR | ID: sea-79741

ABSTRACT

OBJECTIVE: To study the hematological profile of mothers with pregnancy induced hypertension and their infants. METHODS: The effects of maternal hypertension on the hematological profile of neonates were studied in 50 cases comparing the values with that of infants born to normotensive mothers. RESULTS: There was higher number of preterm, Intra-Uterine Growth Restriction (IUGR) and Small for Gestational Age (SGA) babies among the infants of hypertensive mothers. There was a significantly higher incidence of thrombocytopenia and nucleated RBCs seen in these babies. Significant neutropenia was not documented and there was no increased incidence of bleeding when compared to controls. CONCLUSION: Although there were significant changes in the hematological profile of infants born to hypertensive mothers, there was no significant increase in neonatal morbidity as a result of these changes.


Subject(s)
Erythrocyte Indices , Female , Humans , Hypertension, Pregnancy-Induced/blood , Infant, Newborn/blood , Platelet Count , Pregnancy
13.
Indian J Pediatr ; 2005 Jul; 72(7): 557-9
Article in English | IMSEAR | ID: sea-80961

ABSTRACT

OBJECTIVE: This study was carried out to identify the trend and the frequency of neural tube defects from July 1998 to June 2004. METHODS: A total of 310 babies were born with neural tube defects with the overall frequency of 5.7/1000 births compared to 2.3/1000 births observed earlier in our hospital. RESULTS: The most common defect was spina bifida (54.8%) followed by anencephaly (31.6%), and encephalocele (11.6%). More neural tube defects were observed in female and low birth weight babies, still births and unbooked mothers. Neural tube defect was significantly higher among babies born to parents of consanguineous marriage (p< 0.01). Associated congenital defects were observed in thirty nine (12.6%) cases. CONCLUSION: The rise in the frequency of NTDS may indicate the current trend of NTDs in Southern India. A further prospective study is desired to measure the effectiveness of regular folic acid supplementation in bringing down this frequency.


Subject(s)
Consanguinity , Female , Humans , India/epidemiology , Infant, Low Birth Weight , Infant, Newborn , Male , Mothers , Neural Tube Defects/classification , Pregnancy , Prenatal Care , Risk Factors
14.
Indian J Pathol Microbiol ; 2004 Oct; 47(4): 503-5
Article in English | IMSEAR | ID: sea-74367

ABSTRACT

The objective of the study was to assess nucleated red blood cell counts in cord blood in a group of asphyxiated infants, and to determine its predictive value for short-term outcome. A prospective case control study was undertaken on cord blood samples collected from fifty six term neonates with perinatal asphyxia and an equal number of normal appropriately matched controls for cord blood pH and nucleated RBC counts. Babies were followed up in nursery till discharge. Statistical analysis employed were ANOVA test, logistic and linear regression analysis. There was a significant increase in the number of nucleated red blood cells in cases as compared to controls. Low Apgar, cord blood pH and neonatal outcome correlated well with nucleated RBC counts. Nucleated red blood cell count at birth is a useful predictor of severity and short-term outcome of perinatal asphyxia.


Subject(s)
Apgar Score , Asphyxia Neonatorum/blood , Case-Control Studies , Erythroblasts/pathology , Erythrocyte Count , Fetal Blood/cytology , Humans , Infant, Newborn , Prognosis , Prospective Studies
15.
Indian Pediatr ; 2003 Jan; 40(1): 56-9
Article in English | IMSEAR | ID: sea-7357

ABSTRACT

A 10-year-old male child presented with multiple lymph node swellings. A diagnosis of Hodgkins disease was made on histopathological examination. The patient developed relapse six months after his last chemotherapy as a solitary bone tumor, which is rare. Immunohistochemical evaluation helped for the correct typing of Hodgkins disease.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Biopsy , Bone Neoplasms/pathology , Child , Hodgkin Disease/pathology , Humans , Humerus/surgery , Immunohistochemistry , Male , Neoadjuvant Therapy , Neoplasm Recurrence, Local/pathology , Reed-Sternberg Cells/pathology , Treatment Outcome
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