Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Euden Bhutia"'
Publikováno v:
Iranian Journal of Medical Sciences, Vol 42, Iss 4, Pp 416-419 (2017)
Holt-Oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. Skeletal defects exclusively affect the upper limbs
Externí odkaz:
https://doaj.org/article/fad5a1f8c0664f9a81c9cd89576d7c0f
Publikováno v:
Iranian Journal of Medical Sciences, Vol 42, Iss 3, Pp 310-313 (2017)
Bicuspid aortic valve is traditionally considered an innocuous congenital anomaly. Due to a better and widespread availability of non-invasive imaging techniques, it has come to the fore that 30% of these cases develop complications, viz., valve abno
Externí odkaz:
https://doaj.org/article/aa63b6be4cf34c1fb26d3562ec486bbe
Publikováno v:
Annals of Pediatric Cardiology, Vol 9, Iss 2, Pp 164-166 (2016)
A 13-year-old boy presented with vague musculoskeletal pain and involvement of multiple small and large joints along with axial skeleton for the last 3 years, poorly responsive to aspirin. However, on account of presence of carditis and fulfilment of
Externí odkaz:
https://doaj.org/article/e3109e6fcce94ac0b72548afb99e56a4
Publikováno v:
Heart Asia. 8:30-35
To compare the diagnostic yield of acute rheumatic fever (ARF) by the American Heart Association/ American College of Cardiology (AHA/ACC) 2015 revised Jones criteria with the WHO 2004 and Australian guidelines 2012.Retrospective observational study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1173b4c9b522a22206331ebd0412afaf
https://doi.org/10.1136/heartasia-2015-010709
https://doi.org/10.1136/heartasia-2015-010709
Publikováno v:
Heart, lungcirculation. 27(2)
Background The objective of the study was to describe the clinical characteristics of atypical articular presentations during the initial outbreak and recurrence in patients with acute rheumatic fever (ARF) in the paediatric age group. Methods This w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f33e6a05c5198479e56da64a115ed0bb
https://pubmed.ncbi.nlm.nih.gov/28528779
https://pubmed.ncbi.nlm.nih.gov/28528779
Publikováno v:
Annals of Pediatric Cardiology, Vol 9, Iss 2, Pp 164-166 (2016)
Annals of Pediatric Cardiology
Annals of Pediatric Cardiology
A 13-year-old boy presented with vague musculoskeletal pain and involvement of multiple small and large joints along with axial skeleton for the last 3 years, poorly responsive to aspirin. However, on account of presence of carditis and fulfilment of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3705510ffa387a2a5e5c02f4a6e91b75
https://doi.org/10.4103/0974-2069.180670
https://doi.org/10.4103/0974-2069.180670
Publikováno v:
Journal of Clinical Neonatology. 5:128
Neonatal Marfan Syndrome is a rare congenital abnormality with atypical features of Marfan Syndrome and poor prognosis. Multi-valvular involvement is major cardiac manifestation, and heart failure is the most common cause of death.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b55b806fbca51ba296d8fd49737a1a2f
https://doi.org/10.4103/2249-4847.179928
https://doi.org/10.4103/2249-4847.179928
Publikováno v:
Journal of Clinical Neonatology
A rare case of Jarcho Levin syndrome (JLS) presenting as a lethal progressive respiratory insufficiency in early neonatal period is reported. The neonate had classical features of this syndrome including vertebral segmentation defects, typical costo-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9ee369babcf47d0a7cf57dd00beace9
http://europepmc.org/articles/PMC3982342
http://europepmc.org/articles/PMC3982342
Publikováno v:
African Health Sciences; Vol 14, No 2 (2014); 408-413
Background : It is estimated that about 2.5 million people are living with HIV infection in India. Although antiretroviral drugs have been able to reduce the mortality, these drugs have serious side effects one of which is lipodystrophy syndrome. Mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a28b737b365ede2358f067ed4671ca9
https://doi.org/10.4314/ahs.v14i2.17
https://doi.org/10.4314/ahs.v14i2.17
Publikováno v:
Journal of Clinical Neonatology
Less than 100 cases of primordial dwarfism have been reported worldwide out of which Microcephalic osteodysplastic primordial dwarfism type I comprise about
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ac45dbfeca444067fd95eb397dd22cf
https://doi.org/10.4103/2249-4847.128743
https://doi.org/10.4103/2249-4847.128743