Browsing by Author "Aditi Agarwal"
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PublicationLetter Accidental Dapsone Poisoning and Acute Kidney Injury(Scientific Scholar LLC, 2024) Abhishek Abhinay; Aditi Agarwal; Nitish Kumar; Rajniti Prasad[No abstract available]PublicationLetter Bacteriological Profile and Antibiogram of Ventilator Associated Pneumonia(Springer, 2024) Shiva Manwatkar; Aditi Agarwal; Keerthy Reddy; Brijesh Kumar; Sucheta Barnawal; Anil Kumar Saroj; Sunil Kumar Rao[No abstract available]PublicationLetter Clinical Spectrum of Caroli Syndrome(Springer, 2025) Aditi Agarwal; Ankur Singh; Abhishek Abhinay; Rajniti Prasad[No abstract available]PublicationArticle Masquerading as lymphoma: the accelerated phase of Chediak–Higashi syndrome and its novel mutation(Springer Science and Business Media Deutschland GmbH, 2025) Priyanka Aggarwal; Aditi Agarwal; Sonali Aggarwal; Deepa Rani; Vineeta GuptaChediak-Higashi syndrome (CHS) is a rare autosomal recessive disorder. The clinical presentation may be fatal if these patients develop the catastrophic accelerated phase, i.e., hemophagocytic lymphohistiocytosis (HLH). We report a 2.5-year boy that presented to us with complaints of fever, recurrent cough, glandular neck swelling, and abdominal distension for 6 months. He also had a history of female sibling death (age, 3 years) 3 years ago with similar complaints. On examination, he had light skin and silver hair along with severe pallor, generalized significant lymphadenopathy, severe acute malnutrition, and hepatosplenomegaly. Since the patient’s peripheral blood smear and bone marrow showed giant primary azurophilic granules in lymphocytes and eosinophils and the presence of 5 out of 8 HLH 2004 criteria, i.e., fever, hepatosplenomegaly, pancytopenia, hyperferritinemia, and hypertriglyceridemia, a diagnosis of CHS with HLH was made. However, no hemophagocytosis was observed. A novel homozygous nonsense variant in exon 45 of the LYST gene (chr1:g.235702929G > A) similar to the one found in the elder female sibling and previously reported “likely pathogenic” was discovered, which was identified through genetic testing. This case highlights the importance of genetic testing in diagnosis as well as antenatal counselling. © The Author(s), under exclusive licence to Institute of Plant Genetics Polish Academy of Sciences 2025.PublicationLetter Novel Variations in KIRREL1 Gene and Infantile Onset Nephrotic Syndrome(Scientific Scholar LLC, 2024) Abhishek Abhinay; Aditi Agarwal; Ankur Singh; Nitish Kumar[No abstract available]PublicationLetter Performance of Pediatric Intensive Care Unit (PICU) Before and After the Advancement of Resources Under COVID-19 Emergency Response and Health System Preparedness Package Phase II (ECRP-II): Single Center Experience(Springer, 2025) Chandradeep Srivastav; Shiva Manwatkar; Anil Kumar Saroj; Aditi Agarwal; Swati Kabir; Pradhap Krish; Minketan Sidar; Sunil Kumar Rao[No abstract available]PublicationLetter Performance of Pediatric Intensive Care Unit (PICU) Before and After the Advancement of Resources Under COVID-19 Emergency Response and Health System Preparedness Package Phase II (ECRP-II): Single Center Experience(Springer, 2024) Chandradeep Srivastav; Shiva Manwatkar; Anil Kumar Saroj; Aditi Agarwal; Swati Kabir; Pradhap Krish; Minketan Sidar; Sunil Kumar Rao[No abstract available]PublicationLetter Posterior Reversible Encephalopathy Syndrome with Renal Disease(Springer, 2024) Abhishek Abhinay; Aditi Agarwal; Ankur Singh; Shikhar Garg; Devesh Kumar; Rajniti Prasad; Nitish Kumar[No abstract available]PublicationLetter SLC29A3 Gene Spectrum Disorders in Two Siblings(Springer, 2025) Chandradeep Srivastava; Aditi Agarwal; Swetketu Singh; Mainak Ghosh; Anil Kumar Saroj; Sunil Kumar Rao[No abstract available]