Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Anusree Krishna Mandal"'
Autor:
Atish Kumar Basu, Arijit Chakraborty, Syamaprasad Sit, Jadab Kumar Jana, Swarupananda Maiti, Anusree Krishna Mandal
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 16, Iss 12, Pp SC10-SC13 (2022)
Introduction: Nephrotic syndrome, being one of the common glomerular diseases in the paediatric population, is characterised by massive proteinuria and has a negative impact on thyroid function, necessitating investigation. Aim: To assess the status
Externí odkaz:
https://doaj.org/article/995cecd4315b4f6cbc7395f0d610faeb
Publikováno v:
Cureus.
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :64-67
Background:Aiming to know the mortality spectrum and death rate in a paediatric intensive care unit (PICU) in West Bengal's western region and to see whether it differed from previous studies, we conducted this retrospective study. Aims And Objective
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :53-57
Scrub typhus is an emerging acute undifferentiated febrile illness (AUFI) among children, particularly in rural West Bengal. Due to the lack of gold standard diagnostic tests, and lack of awareness among healthcare personnel, it leads to delay in dia
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :46-48
Childhood diarrhea is one of the major public health problems. Diarrhea is the second most common cause of mortality in under-ve children. Use of Oral rehydration salts (ORS) solution is the most cost-effective intervention to prevent diarrhea rel
Publikováno v:
British Association of General Paediatrics.
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :30-31
Background: Pompe disease is a metabolic disorder due to deciency of lysosomal acid alpha-glucosidase enzyme. Deciency of this enzyme leads to lysosomal glycogen accumulation in multiple tissues and cell types, predominantly affecting cardiac,
Publikováno v:
BMJ Case Reports. 15:e251092
We report a case of congenital dyserythropoietic anaemia (CDA) type II in a female child, which is an extremely rare cause of hereditary anaemia. The patient, still in her early childhood, presented to us with transfusion-dependent anaemia, unexplain
Publikováno v:
BMJ Case Reports. 15:e248930
A female child hailing from South Asia, India presented with pallor, multiple petechiae and ecchymosis. Based on the clinical picture and demography, the differentials considered were pancytopenia of nutritional origin, acute leukaemia, autoimmune an