Results 31 to 40 of about 8,563 (214)

Liver Transplantation in Situs Inversus and Portal Vein Thrombosis (First Case Report in Russia)

open access: yesРоссийский журнал гастроэнтерологии, гепатологии, колопроктологии, 2020
Situs inversus is a rare mirror transposition of internal organs relative to the median plane. Liver transplantation in situs inversus is a serious medical challenge imposed by an abnormal arrangement of the recipient's organs.Aim.
M. S. Novruzbekov   +5 more
doaj   +1 more source

Primary ciliary dyskinesia (Siewert's/Kartagener's syndrome): respiratory symptoms and psycho-social impact

open access: yes, 2003
Although the pathophysiological defect in primary ciliary dyskinesia (PCD; Siewert's/Kartagener's syndrome) is now well characterised, there are few studies of the impact of the condition upon health function, particularly in later life.
I Christopher McManus   +14 more
core   +1 more source

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill [PDF]

open access: yes, 2013
This work was supported by the University of St Andrews, the UK Medical Research Council (grant number G0800523/86473 to SP), the Max Plank Society, and the the EU (Neurodys, 018696).
Timpson, NJ   +108 more
core   +1 more source

Cholecystitis in situs inversus totalis

open access: yes, 2019
A 20-year-old male presented to Nambour General Hospital Emergency Department with a 24-h history of left upper quadrant and epigastric pain, nausea, vomiting and fever. The patient had no significant medical or surgical history other than being known to
Copertino, NJ, Grieve, D
core   +1 more source

Colecistite calculosa em situs inversus totalis: abordagem laparoscópica [PDF]

open access: yes, 2019
Introduction: Situs inversus is a rare congenital anomaly characterized by transposition of the abdominal organs, viscera and vasculature, in relation to the sagittal direction, offering an image called “mirror image”.
Andrade, Mariana Alma Rocha de   +8 more
core   +1 more source

Acute gastrointestinal manifestation of situs inversus abdominus

open access: yes, 2017
Purpose: Whilst situs inversus is associated with intestinal malrotation and volvulus particularly in infants, this is the first known report of acute intestinal obstruction in an adult patient with a situs anomaly specifically due to a congenital ...
Gundara, JS, Mittal, A, Brown, KM
core   +1 more source

Liver and pancreas transplantation in adult donor and recipients with situs inversus totalis: a case series and review of the literature

open access: yesJournal of Medical Case Reports
Background Situs inversus totalis is a rare congenital anomaly characterized by a mirror-image orientation of abdominal, and in some cases, thoracic organs.
Alireza Shamsaeefar   +11 more
doaj   +1 more source

Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy   +16 more
wiley   +1 more source

Cor triatriatum sinister with situs inversus totalis in an infant. [PDF]

open access: yes, 2012
Cor triatriatum sinister is a rare congenital cardiac malformation characterized by a membrane in the left atrium which separates the left atrium into the proximal and distal chambers.Association of cor triatriatum is extremely rare with situs inversus
Taksande, Amar M.   +3 more
core  

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena   +13 more
wiley   +1 more source

Home - About - Disclaimer - Privacy