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Ebstein anomaly is a congenital malformation of the heart that is characterized by apical displacement of the septal and posterior tricuspid valve leaflets, leading to atrialization of the right ventricle with a variable degree of malformation and displacement of the anterior leaflet.
giant systolic pulsations, known as C-V waves, were noticeable during jugular venous examination of a 33-year-old woman who had tricuspid-valve endocarditis. In video 2, transthoracic echocardiography revealed severe tricuspid regurgitation.
Orthognathic surgery presented in this video in order of appearance. 1. Advancement Genioplasty 2. Maxillary Advancement 3. Maxillary impaction 4. BSSO Mandibular Advancement 5. BSSO Mandibular Set-back 6. Maxillary Posterior Impaction
Overbite is a type or malocclusion or an overjet. A lot of people don’t realize that they have an overbite, as they believe their condition is not serious enough to obtain dental attention. This could also for the reason that other cases of overbites are so minor to be noticeable. However, others have serious overbite condition that can make the person’s top jaw look much larger or the bottom jaw significantly smaller. But one thing to remember, overbite can actually cause some dental problems. This condition can change the structure of your face and affect the way you talk. The most popular form of overbite correction is orthodontic treatment. Your dentist will fix the overbite with the help of rubber bands and dental braces to pull the upper teeth back. Tooth extraction may be suggested if overcrowding complicates the overbite so as to provide room for your front teeth. In extreme conditions, overbite surgery may be needed to place your jaw backwards or forwards. Furthermore, if severe overbite is not corrected during adulthood, the teeth may continue to shift and trigger dental issues such as gum disease.
Alcohol septal ablation (ASA, TASH, Sigwart procedure) is a percutaneous, minimally-invasive treatment performed by an interventional cardiologist to relieve symptoms and improve functional status in severely symptomatic patients with hypertrophic cardiomyopathy (HCM) who meet strict clinical, anatomic and physiologic ...
Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, beginning in their first two years of life. Children with progeria generally appear normal at birth. During the first year, signs and symptoms, such as slow growth and hair loss, begin to appear. Heart problems or strokes are the eventual cause of death in most children with progeria. The average life expectancy for a child with progeria is about 13 years, but some with the disease die younger and some live 20 years or longer. There's no cure for progeria, but ongoing research shows some promise for treatment.
Chalazions are extremely common, and having a sound surgical technique to drain a chalazion is a fundamental in general ophthalmology and oculoplastic surgery. I believe one of the biggest downfalls in treating chalazions is inadequate local anesthetic. Please that both the outer and inner surface to the eyelid need to receive local anesthesia to make the patient totally comfortable. It is important to be careful in delivering the local anesthetic and making sure you have control of the head position, and the position of your needle is bent to minimize any possibility of contact with the globe.
For education, Microsoft HoloLens will help make incredible leaps forward in productivity, collaboration, and innovation. See how Microsoft HoloLens transforms the way we teach anatomy and our understanding of the human body as we help to prepare the next generation of doctors.
The cause of pectus excavatum is not known however it can run in families, with up to 25 percent of affected patients reporting chest wall abnormalities in other family members. Pectus excavatum occurs in approximately 1 out of 400–1000 children and is three to five times more common in males than females.
The cause of pectus excavatum is not known however it can run in families, with up to 25 percent of affected patients reporting chest wall abnormalities in other family members. Pectus excavatum occurs in approximately 1 out of 400–1000 children and is three to five times more common in males than females.