Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Priyanshu Mathur"'
Publikováno v:
Journal of Pediatric Critical Care, Vol 5, Iss 1, Pp 36-38 (2018)
Hypohydrotic ectodermal dysplasia (HED) is characterized by classical triad of Hypotrichosis (sparseness of scalp and body hair), anhidrosis/hypohidrosis (absence or reduction of sweat glands), and hypodontia/ anodontia (congenital absence of teeth).
Externí odkaz:
https://doaj.org/article/c746fd88a3584a76981c8fe836f35c8b
Publikováno v:
Journal of Pediatric Critical Care, Vol 3, Iss 3, Pp 69-72 (2016)
Wegener’s granulomatosis is an uncommon autoimmue disease with multi-system involvement, characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tracts and general focal necrotizing vasculitis (Commonly known as W
Externí odkaz:
https://doaj.org/article/13784cf9050843c88325d47f9e3dfb21
Publikováno v:
Journal of Pediatric Critical Care, Vol 4, Iss 4, Pp 100-102 (2017)
The C-V junction is a transition site between mobile cranium and relatively rigid spinal column. It is also the site of the medullo-spinal junction. CV anomalies are defects of development, not necessarily congenital and may not manifest at birth. Th
Externí odkaz:
https://doaj.org/article/e08be4f8f8cf412f8f3a6e1518b0c691
Autor:
Manisha Garg, Ashok Gupta, Priyanshu Mathur, Manish Sharma, Rajesh Kumar, Vikas Gupta, M Manjunath
Publikováno v:
Journal of Pediatric Critical Care, Vol 3, Iss 3, Pp 66-68 (2016)
Fanconi-Bickel syndrome (FBS) is an example of proximal Renal tubular dysfunction due to a single gene disorder, it is caused by defects in the facilitative glucose transporter 2 gene that codes for the glucose transporter protein 2 expressed in hepa
Externí odkaz:
https://doaj.org/article/769de4ea9e7c40a4914f1344289342c6
Publikováno v:
Journal of Pediatric Critical Care, Vol 3, Iss 2, Pp 61-63 (2016)
The Landau-Kleffner syndrome or the syndrome of acquired epileptic aphasia was first described in 1957. The disorder is characterized by gradual or rapid loss of language in a previously normal child. Acquired epileptic aphasia (AEA) typically develo
Externí odkaz:
https://doaj.org/article/fbaf5806b6904c9a9963416168d77347
Publikováno v:
Journal of Pediatric Critical Care, Vol 3, Iss 4, Pp 115-117 (2016)
The oral-facial-digital syndromes (OFDS) are rare genetic heterogenous group of disorders characterized by oral (mouth and teeth), facial and digital (fingers and toes) anomalies. OFDS are classified into 13 potential forms. OFDS Type II (Mohr syndro
Externí odkaz:
https://doaj.org/article/b152b0ab21c6483d8a9608dc95de9ffe
Publikováno v:
Case Reports in Pediatrics, Vol 2016 (2016)
Epilepsy is a common disorder and exposure to antiepileptic drugs during pregnancy increases the risk of teratogenicity. Older AEDs such as valproate and phenobarbital are associated with a higher risk of major malformations in the fetus than newer A
Externí odkaz:
https://doaj.org/article/558ef36d8ae74e5aa3b21a576da60d13
Autor:
Praveen Mathur, Priyanka Udawat, Priyanshu Mathur, Dilip Ramrakhiani, Sandeep K. Mathur, S. Sitaraman, R. K. Gupta, Saurav Sultania, Reshu Gupta
Publikováno v:
Indian journal of pediatrics. 89(7)
Publikováno v:
IOSR Journal of Dental and Medical Sciences. 15:53-58
Objective: To assess the attitude of parents and child asa barrier to dietary compliance in celiac disease. Methods: 100 parents and 100 children were assessed for dietary compliance with the questionnaire based interview. The assessment of psychosoc
Publikováno v:
Scholars Journal of Applied Medical Sciences. 4:1981-1985
The objective of this paper was to compare the efficacy of chloroquine and co-artemether in uncomplicated malaria cases. It was a prospective interventional study. The subjects included children with PBF proven uncomplicated Malaria (n=49) admitted i