Results 51 to 60 of about 26,309 (240)

Control of Disabling Vertigo in Ménière’s Disease Following Cochlear Implantation without Labyrinthectomy

Audiology Research, 2022
Background: The placement of a cochlear implant (CI) can restore auditory function in the case of profound cochlear deafness, which may be due to Ménière’s disease (MD) or be associated with symptoms related to endolymphatic hydrops.
Andrea Canale, Giulia Dalmasso, Roberto Albera, Sergio Lucisano, George Dumas, Flavio Perottino, Andrea Albera   +6 more
doaj   +1 more source

Ménière's Disease: A Tri‐Decade Scoping Review of Treatment Trends and Evidence Quality

The Laryngoscope, EarlyView.
This tri‐decade scoping review of Ménière's disease literature reveals a significant increase in high‐level evidence and a clinical pivot toward hearing‐preserving interventions, such as intratympanic steroids and cochlear implants. However, a significant quality paradox has emerged, where adherence to standardized AAO‐HNS reporting and diagnostic ...
Ofir Zavdy, Teeraya Piyajarawong, Seamus Boyle, Ross O'Shea, John Rutka   +4 more
wiley   +1 more source

Ultrasound of the Gallbladder—An Update on Measurements, Reference Values, Variants and Frequent Pathologies: A Scoping Review

Life
Objective: We aimed to provide an update on ultrasound measurements of the gallbladder with studies focusing on measurement techniques, reference values, and influencing factors.
Claudia Lucius, Barbara Braden, Christian Jenssen, Kathleen Möller, Michael Sienz, Constantinos Zervides, Manfred Walter Essig, Christoph Frank Dietrich   +7 more
doaj   +1 more source

Heterozygous Beta‐Thalassaemia in Pregnancy: Two Rare Causes of Severe Fetal Anemia Requiring Intrauterine Blood Transfusions

Prenatal Diagnosis, EarlyView.
ABSTRACT Aim In this article, we present two cases of severe fetal hemolytic anemia based on a beta‐thalassaemia trait inherited from a single parent. Results These cases, presented at 20 and 28 weeks' gestation, necessitated intra‐uterine blood transfusions.
Eva van der Meij, Frans J. W. Smiers, Tamara T. Koopmann, Ingrid Krapels, Kaatje LePoole, Enrico Lopriore, Johanna M. Middeldorp, Claudia S. Ootjers, Volkher Scharnhorst, Hubertina C. J. Scheepers, Cornelis L. Harteveld, E. J. T. (Joanne) Verweij   +11 more
wiley   +1 more source

Spontaneous Corneal Clearing after Descemet Membrane Rupture and Near-Total Detachment in Keratoglobus: A Case Report

Case Reports in Ophthalmology
Introduction: We present a case of a patient with osteogenesis imperfecta (OI) and keratoglobus (KG) who had a near-total rupture of Descemet’s membrane followed by spontaneous corneal clearing. This case is unique in that it demonstrates the potentially
Hanel W. Eberly, David B. Rosen, Seth M. Pantanelli   +2 more
doaj   +1 more source

First Reported Case of Hydrops Foetalis Following Critical Phase Maternal Dengue Haemorrhagic Fever

Sri Lanka Journal of Medicine, 2022
We report a case of hydrops foetalis due to maternal dengue haemorrhagic fever (DHF).  A 19-year-old mother was diagnosed to have DHF with positive NS1 Antigen (NS1) at 39 weeks of gestation. Ultrasound scan revealed fetal hypoxia.
R. A. S. P. Gunarathna, M. H. S. M. Hassan, H. Vigneswararjha, M. N. Lucus   +3 more
doaj   +1 more source

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

Prenatal Diagnosis, EarlyView.
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell, Samantha Stover, Nora Gibson, Timothy Olson, James Connelly, Matthew Grace, Jennifer Andrews   +6 more
wiley   +1 more source

Intratympanic Gentamicin Injection for Endolymphatic Hydrops After Cochlear Implantation

Endolymphatic hydrops has been documented as a possible complication of cochlear implantation; however, few studies have addressed its treatment.
Ilaria Ottoboni, Elena Carlotto, Cesare Chiapperini, Quaglieri, Silvia, Carlotto, Elena, Silvia Quaglieri, Minervini, Domenico, Maurizio Guida, Domenico Minervini, Benazzo, Marco, Guida, Maurizio, Stellato, Anna Chiara, Chiapperini, Cesare, Manfrin, Marco Lucio, Anna Chiara Stellato, Marco Lucio Manfrin, Marco Benazzo, Pietro Canzi, Canzi, Pietro, Ottoboni, Ilaria   +19 more
core   +1 more source

Hydrops foetalis

, 2022
Congenital hydrops fetalis describes an abnormal accumulation of fluid in two or more compartments in a fetus. The disease is categorized based on the aetiology: immune- and non-immune hydrops fetalis. Today, the nonimmune form is the most common.
Jepsen, Agnete Runge, Breindahl, Morten, Hamran, Kristine, Hansen, Bo Mølholm, Gjørup, Vibike, Westergaard, Hanne Brix   +5 more
core  

Hemolytic Disease of the Fetus and Newborn: Fetal RHD Genotyping, Targeted Prophylaxis, and Prenatal Therapies

Prenatal Diagnosis, EarlyView.
ABSTRACT Hemolytic disease of the fetus and newborn (HDFN) remains a significant concern in prenatal care primarily caused by maternal alloimmunization against fetal red blood cell antigens, most commonly the D antigen. Noninvasive fetal RHD genotyping, used as a screening tool, enables targeted antenatal prophylaxis and has been implemented in several
Emilie Thorup, Steffen Thorsen, Morten Hanefeld Dziegiel, Olav Bjørn Petersen, Frederik Banch Clausen   +4 more
wiley   +1 more source