Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Himanshu Barman"'
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 22, Iss 3, Pp 397-404 (2018)
Introduction: Hypokalemia is associated with increased morbidity and at times mortality. “Hypokalemic paralysis”, particularly if recurrent, has often been considered synonymous with “hypokalemic periodic paralysis (HPP)”; however, diseases s
Externí odkaz:
https://doaj.org/article/439efd369429426ab8793533a036cd19
Publikováno v:
BMJ Case Rep
An 8½-year-old adopted girl presented to her paediatrician with bowing of her legs and cafe-au-lait macules and was referred to us with a working diagnosis of rickets in McCune-Albright syndrome (MAS). Clinical examination revealed genu valgum, wide
Patients with mucopolysaccharidoses (MPS) have a plethora of multisystemic manifestations depending on the particular type, and atypical presentations are not uncommon. MPS type IVA (Morquio A syndrome) has predominant musculoskeletal system involvem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40092dd21336afe1e19823253bd5820d
https://europepmc.org/articles/PMC5665360/
https://europepmc.org/articles/PMC5665360/
Publikováno v:
BMJ case reports. 2017
A 22-year-old man, detected to have type 1 diabetes at the age of 9 years, presented with left-sided frontotemporal headache for 1 week followed by left-sided ptosis and binocular diplopia for 4 days. The headache was deep seated and his ocular compl
Publikováno v:
BMJ case reports. 2016
A 14-year-old girl without diabetes presented with recurrent attacks of generalised tonic–clonic seizures for the past 3 years which had partially been controlled with phenytoin and not with sodium valproate or levetiracetam. A detailed history rev
Publikováno v:
BMJ Case Rep
A 19-year-old nulliparous eumenorrhoeic woman diagnosed with bilateral serous retinal detachment was referred for incidentally detected enlarged pituitary gland, seen on MRI of orbit. A focused MRI documented diffuse, symmetric enlargement of the pit
Publikováno v:
BMJ Case Reports. :bcr-2017
Mutations in hepatocyte nuclear factor-1β gene result in a multisystemic syndrome where a monogenic form of diabetes (maturity-onset diabetes of young type 5; MODY 5) and renal anomalies, usually bilateral multiple cysts are the most characteristic
Publikováno v:
BMJ Case Reports. :bcr-2018
A 7-year-old boy, born of a non-consanguineous union, presented with pain over both hips and progressive difficulty in walking for preceding 2 years. He had normal developmental milestones with satisfactory scholastic performances and his family and
Autor:
Gouranga Santra, Himanshu Barman
Publikováno v:
Journal of Current Research in Scientific Medicine. 3:45
Introduction: Studies describing etiological distribution of tetany are rare, and awareness regarding it is poor among physicians. Our study describes different causes of tetany beyond the decrease in total serum calcium level. Methods: Patients with