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Autor:
V.P. Myneedu, M V V Rao, Soumya Swaminathan, Anant Mohan, Rohit Sarin, Anuj Bhatnagar, Jyoti Logani, Raman R. Gangakhedkar, Jiten Singh Khangembam, T Kannan, Urvashi B. Singh, Devendra Singh Chauhan, N S Gomathi, Bindu Dey, Manjula Singh, Srikanth Tripathy
Publikováno v:
Indian Journal of Medical Research, Vol 152, Iss 5, Pp 482-489 (2020)
The Indian Journal of Medical Research
The Indian Journal of Medical Research
Background & objectives: There is a need for an affordable, easy, high-sensitivity test usable at the peripheral health facility for diagnosis of drug-resistant (DR) tuberculosis (TB) to interrupt disease transmission. Nucleic acid amplification test
Publikováno v:
Scientific Dental Journal, Vol 4, Iss 3, Pp 142-147 (2020)
Background: Older persons are at risk of compromised oral conditions, including dental infections, periodontal problems, tooth loss, benign mucosal lesions, xerostomia, oral candidiasis, and oral cancer. Poor oral hygiene has contributed to increase
Autor:
Chinedu John-Camillus Igboanusi, Benjamin Olatubosun, Awawu Grace Nmadu, Istifanus Anekoson Joshua, Mary O Onoja-Alexander
Publikováno v:
Sahel Medical Journal, Vol 23, Iss 3, Pp 184-190 (2020)
Background: Neonatal jaundice (NNJ) is a common cause of hospitalization in the 1st week of life and a significant cause of neonatal morbidity and mortality worldwide. Objectives: The aim of this study was to assess the knowledge and attitude related
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 2, Pp 524-527 (2020)
Hyperkalemia is one of the dangerous complications of renal impairment (acute kidney injury or chronic kidney disease). Hyperkalemia may present with the electrocardiogram (ECG) changes as nonspecific repolarization abnormalities. Here, we report a c
Publikováno v:
Clinical Dermatology Review, Vol 4, Iss 1, Pp 57-60 (2020)
Ross syndrome is a rare disorder of sweating with a triad of segmental anhidrosis, tonic pupil, and hyporeflexia. Survey of available literature shows scarce reporting of such cases globally and countable number of cases from India. Here, we report t
Autor:
Azza F Alhelo, Soulafa A Almazrooa, Ghada A Mansour, Sana A Alhamed, Sara Alfarabi, Sara K Akeel, Nada O Binmadi, Nada A Alhindi, Lujain Alsulaimani, Manal A Alamri, Hani H Mawardi
Publikováno v:
Saudi Journal of Oral Sciences, Vol 7, Iss 3, Pp 199-205 (2020)
Introduction: Lichen planus (LP) is a common chronic, mucocutaneous inflammatory disorder with unclear pathophysiology. The aim was to describe the epidemiology and clinicopathological characteristics of oral lichen planus (OLP) patients at King Abdu
Publikováno v:
International Journal of Noncommunicable Diseases, Vol 5, Iss 2, Pp 83-89 (2020)
For most individuals, the coronavirus disease 2019 (COVID-19) pandemic is a novel and anxiety provoking experience. With ongoing outbreaks in many regions around the globe, it has led to worldwide social distancing measures, travel restrictions, job
Publikováno v:
Brain Circulation, Vol 6, Iss 4, Pp 225-241 (2020)
Brain Circulation
Brain Circulation
Neurocysticercosis (NCC) is a specific form of cysticercosis that affects the central nervous system. It is caused by the tapeworm Taenia solium, which is often found in pigs. NCC is considered one of the “great simulator/mimickers” of other dise
Autor:
Mudasir Nazir, Bilal Ahmad Bhat, Shanoo Sheikh, Aaliya Khanam, Zaid Ahmad Wani, Junaid Nabi, Deeba Nazir, Shabir Ahmad Dar
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 13, Iss 1, Pp 37-42 (2020)
Background: Menopausal transition (MT) is the period of irregular menstrual activity which directly precedes menopause and is characterized by widely fluctuating hormone levels and reproductive, metabolic, and psychological disturbances. We aimed to
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 8, Iss 2, Pp 146-150 (2020)
Saudi Journal of Medicine & Medical Sciences
Saudi Journal of Medicine & Medical Sciences
Crouzon syndrome is a rare genetic disorder. We report a rare case of Crouzon syndrome in a very young infant with distinct features of craniofacial malformations. A 10-week-old male child presented with features of craniofacial dysostosis with abnor