Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Devdeep Mukherjee"'
Autor:
Sunetra Mondal, Lakshmi Nagendra, Amarta S. Chowdhury, Rajan Palui, Soumyadeep Biswas, Devdeep Mukherjee, Krishnendu Khan, Aritra Sengupta, Anupama Pandey
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 2, Pp 145-152 (2024)
Introduction: Infants born preterm, with low birth weight (LBW), or with perinatal stress are at high risk for neonatal hypoglycemia. Low cortisol levels have also been demonstrated in this group of neonates, which is often transient. We report a ser
Externí odkaz:
https://doaj.org/article/e250726c808f464b84090f444120d332
Autor:
Satyajit Das, Gopikrishna Kursa, Sukalyan Purkayastha, Subrata Nag, Ashok Bharati, Devdeep Mukherjee
Publikováno v:
Archives of Pediatric Neurosurgery, Vol 5, Iss 2, Pp e1722023-e1722023 (2023)
Background: Spinal vascular malformations (SVM) are a complex entity and rarely noted in children. They are commonly seen in the elderly with a predilection for the thoraco-lumbar region. The incidence varies from 3-11% and varies across all age grou
Externí odkaz:
https://doaj.org/article/977ee6795228422f945b3157ba75284b
Autor:
Ishita Majumdar, Hemant Kumar Nayak, Rajarshi Ghosh, Srirup Chatterjee, Prithwish Roy, Devdeep Mukherjee
Publikováno v:
Annals of Pediatric Cardiology, Vol 16, Iss 1, Pp 71-73 (2023)
Primary chylopericardium (PC) is a rare entity in the pediatric population with very few reported cases. Most cases of chylopericardium manifest after trauma or following cardiac surgery. The other etiologies which may lead to chylopericardium are ma
Externí odkaz:
https://doaj.org/article/7267ec24e74c4bd0931a05342341e930
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 10, Iss 2, Pp e100201-e100201 (2021)
Factor XIII deficiency is an autosomal recessive disorder with an incidence of 1 in 1-5 million. On activation factor XIII stabilizes clot formation by cross-linking fibrin strands. Deficiency is characterized by severe bleeding due to impairment in
Externí odkaz:
https://doaj.org/article/90a2afea658a474b96138a039a21b16b
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 18, Iss 4, Pp 338-340 (2017)
Henoch–Schonlein purpura (HSP) with facial involvement with bullous rashes are extremely rare. A 12-year-old boy presented with abdominal pain and features of arthritis. He also had multiple purpuric rashes over his lower limbs. Gradually, he devel
Externí odkaz:
https://doaj.org/article/23cca1b6899b4b41b833b94f4f939804
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 17, Iss 1, Pp 45-47 (2016)
Central nervous system involvement in segmental nevus depigmentosus (SND) is rare. A 7-month-old boy having convulsion and segmental hypopigmented patch in the right inguinal region. Magnetic resonance imaging of brain showed bilateral periventricula
Externí odkaz:
https://doaj.org/article/04d9adb141b045f8af24fe3ae296f9aa
Publikováno v:
Journal of Pediatric Critical Care, Vol 3, Iss 2, Pp 52-54 (2016)
Staphylococcal toxic shock syndrome (TSS) is a rare and potentially fatal multi system dysfunction. The syndrome occurs primarily due to TSS Toxin-1 (TSS-1) liberated by Staphylococcus aureus (SA). Fever with rash followed by multi organ dysfunction
Externí odkaz:
https://doaj.org/article/7d33d2305dd4406da6d56c4d88a925ec
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 6, Iss 2, Pp e060216-e060216 (2017)
Ascariasis is endemic in India and is common in areas of poor sanitation. The most common complications are intestinal and biliary ascariasis, which are associated with significant morbidity. We report a 7-month-old child who presented with obstructi
Externí odkaz:
https://doaj.org/article/964fea0006c2413686c924af4cb889e1
Publikováno v:
Journal of Krishna Institute of Medical Sciences University, Vol 4, Iss 1, Pp 139-141 (2015)
Friedreich's ataxia (FA) is an autosomal recessive spinocerebellar degenerative disease characterized by hyperexpansion of GAA triplets in Frataxin gene. The hallmark of this disorder is ataxic gait, areflexia, Babinski's sign and positive Romber
Externí odkaz:
https://doaj.org/article/e526800a09df4e4289efb7f06ae5a240
Publikováno v:
Journal of Krishna Institute of Medical Sciences University, Vol 03, Iss 01, Pp 104-106 (2014)
Hyper IgM syndrome is a rare genetically heterogenous syndrome and is characterized by an elevated or normal serum IgM and decreased IgG, IgA and IgE, indicating a defect in the class – switch recombination (CSR) process. Patients are prone to
Externí odkaz:
https://doaj.org/article/f7d8ed61b2724ec1a5c971f7c9145a89