Aaradhana Singh
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View article: Hidden Hearing Loss (Cochlear Synaptopathy): Diagnostic Challenges and Emerging Tests
Hidden Hearing Loss (Cochlear Synaptopathy): Diagnostic Challenges and Emerging Tests Open
Hidden hearing loss (HHL), often attributed to cochlear synaptopathy, is characterized by difficulty understanding speech in noisy environments despite clinically normal pure-tone thresholds. Moderate noise exposure or aging may destroy sy…
View article: Coexistence of Spinal Intramedullary and Intracranial Tuberculomas in a Child with Hemiparesis: A Case Report with Review of Literature
Coexistence of Spinal Intramedullary and Intracranial Tuberculomas in a Child with Hemiparesis: A Case Report with Review of Literature Open
Background: While isolated spinal intramedullary tuberculomas are very rare, concurrent occurrence with intracranial tuberculoma is even more rare. Clinical Description: An 11-year-old, developmentally normal girl, presented with fever and…
View article: Adrenal Insufficiency after Steroid Therapy in Children with Steroid-Sensitive Nephrotic Syndrome: A Cross-sectional Study
Adrenal Insufficiency after Steroid Therapy in Children with Steroid-Sensitive Nephrotic Syndrome: A Cross-sectional Study Open
Introduction: Glucocorticoid-induced adrenal insufficiency (AI) is underestimated and under-reported in children with nephrotic syndrome (NS). This study aimed to estimate the prevalence of AI in children with steroid-sensitive NS, defined…
View article: THE COMPREHENSIVE STUDY ON CONGENITAL CHALLENGES In IVF NEWBORNS
THE COMPREHENSIVE STUDY ON CONGENITAL CHALLENGES In IVF NEWBORNS Open
View article: Moyamoya Syndrome in a Child with Beta-Thalassemia Trait: A Case Report with Review of Literature
Moyamoya Syndrome in a Child with Beta-Thalassemia Trait: A Case Report with Review of Literature Open
Background: The association of moyamoya angiopathy with hematological conditions such as sickle cell anemia and beta-thalassemia major or intermedia is well-known, but moyamoya syndrome (MMS) associated with thalassemia trait is hardly rep…
View article: Quality of Life of Developmentally Normal Children With Epilepsy and Their Siblings
Quality of Life of Developmentally Normal Children With Epilepsy and Their Siblings Open
View article: Immunogenicity of measles-rubella vaccine administered under India’s Universal Immunization Programme in the context of measles–rubella elimination goal: A longitudinal study
Immunogenicity of measles-rubella vaccine administered under India’s Universal Immunization Programme in the context of measles–rubella elimination goal: A longitudinal study Open
Background & objectives: There is a paucity of data regarding immunogenicity of recently introduced measles–rubella (MR) vaccine in Indian children, in which the first dose is administered below one year of age. This study was undertaken t…
View article: Emphysematous osteomyelitis of the spine with emphysematous pyelonephritis: A rare coexistence
Emphysematous osteomyelitis of the spine with emphysematous pyelonephritis: A rare coexistence Open
Department of General Medicine, Government Medical College and Hospital, Chandigarh, India 1Department of Radiodiagnosis, Government Medical College and Hospital, Chandigarh, India Address for correspondence: Mr. Singh A, E-mail: [email pr…
View article: 50 Years Ago in
50 Years Ago in Open
View article: Profile of adverse events following immunization with measles rubella vaccine at a tertiary care hospital in East Delhi, India
Profile of adverse events following immunization with measles rubella vaccine at a tertiary care hospital in East Delhi, India Open
Background: As a part of a measles and rubella (MR) campaign, the MR vaccine replaced the two-dose measles vaccine at 9–12 months and 16–24 months of age under the Universal Immunization Program (UIP). Although adverse events following imm…
View article: Subacute sclerosing panencephalitis in a child with celiac disease – A rare association
Subacute sclerosing panencephalitis in a child with celiac disease – A rare association Open
Celiac disease (CD) is an immune-mediated disease with varied intestinal and extraintestinal manifestations. Among extraintestinal manifestations, neurological conditions are being reported with increased frequency nowadays. We report a ch…
View article: VISUAL IMPAIRMENTS IN CHILDREN WITH CEREBRAL PALSY
VISUAL IMPAIRMENTS IN CHILDREN WITH CEREBRAL PALSY Open
Background: Visual impairments are associated with cerebral palsy (CP). They enhance functional limitations in children with CP. Objective: The objective of the study was to determine the types of visual impairments in children with CP, an…
View article: RARE ASSOCIATION OF CELIAC DISEASE WITH CONGENITAL HEART DISEASE
RARE ASSOCIATION OF CELIAC DISEASE WITH CONGENITAL HEART DISEASE Open
View article: Rare association of celiac disease with congenital heart disease
Rare association of celiac disease with congenital heart disease Open
Celiac disease (CD) is an autoimmune enteropathy caused by exposure to dietary gluten in genetically predisposed individuals. CD is a multisystem disease involving gastrointestinal, hepatobiliary, nervous, hematologic, and cardiovascular s…
View article: Profile of acute childhood poisoning at a tertiary care teaching hospital in North India
Profile of acute childhood poisoning at a tertiary care teaching hospital in North India Open
Objective: The objective of the study was to determine the profile and outcome of children under the age of 12 years admitted with acute poisoning at a tertiary care teaching hospital in Delhi. Materials and Methods: We retrospectively rev…
View article: Waardenburg syndrome-associated focal segmental glomerulosclerosis: A rare presentation
Waardenburg syndrome-associated focal segmental glomerulosclerosis: A rare presentation Open
Waardenburg syndrome (WS) is characterized by auditory and pigmentary disorders with an incidence of 1:40,000. Renal involvement is rare in WS. A 10-year-old male, diagnosed as nephrotic syndrome at 4 years, was presented in relapse. A ren…
View article: Congenital Cytomegalovirus Infection Presenting as Severe Conjugated Hyperbilirubinemia on First Day of Life
Congenital Cytomegalovirus Infection Presenting as Severe Conjugated Hyperbilirubinemia on First Day of Life Open
Congenital Cytomegalovirus infection (CMV) has varied presentations ranging from asymptomatic to involvement of multiple organ systems like central nervous system, gastrointestinal, hepatic and hematopoietic. Jaundice is a manifestation of…
View article: The effect of nutritional status on the response to highly active antiretroviral therapy in human immunodeficiency virus-infected children at regional antiretroviral therapy centre in Northern India
The effect of nutritional status on the response to highly active antiretroviral therapy in human immunodeficiency virus-infected children at regional antiretroviral therapy centre in Northern India Open
Background: Effect of highly active antiretroviral therapy (HAART) on growth in children is well established but influence of prior nutritional status on the response to HAART is not well known. Objective: To determine the influence of pri…
View article: SCIMITAR SYNDROME - A RARE CAUSE OF RECURRENT PNEUMONIA
SCIMITAR SYNDROME - A RARE CAUSE OF RECURRENT PNEUMONIA Open
Scimitar syndrome is a congenital anomaly characterized by anomalous drainage of the right lung into inferior vena cava. This may be associated with other anomalies in the form of pulmonary hypoplasia, systemic arterial supply of right lun…
View article: Predictors of neonatal mortality referred to a tertiary care teaching institute: A descriptive study
Predictors of neonatal mortality referred to a tertiary care teaching institute: A descriptive study Open
Objective: To assess the predictors of neonatal mortality transported to our institution from other hospitals. Methods: In this descriptive study, neonates who were delivered outside of the hospital premises and were referred to our tertia…
View article: Moebius Syndrome in an Infant with Fetal Misoprostol and Mifepristone Exposure
Moebius Syndrome in an Infant with Fetal Misoprostol and Mifepristone Exposure Open