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Chest x-ray of a five-year-old girl with Scimitar syndrome. The heart (blue outline) is shifted into the right half of the chest, and the anomalous pulmonary venous return (red) has a shape reminiscent of a Scimitar. The diagnosis is made by transthoracic or transesophageal echocardiography [citation needed] and selective pulmonary angiography. [5]
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Print/export Download as PDF ... Radiologic signs are the signs used for diagnosing physiological and pathological conditions in radiologic images. This list includes ...
Schöpf–Schulz–Passarge syndrome; Scimitar syndrome; Scott syndrome; Seaver Cassidy syndrome; Seckel syndrome; Second-impact syndrome; Secretan's syndrome; Seed dispersal syndrome; Senior–Løken syndrome; Sensenbrenner syndrome; Septo-optic dysplasia; Serkal syndrome; Serotonin syndrome; Serpentine fibula-polycystic kidney syndrome ...
3.3 per 100,000 (adults), 50 per 100,000 (children) [90] Thrombotic thrombocytopenic purpura: ADAMTS13 autoantibodies Confirmed 1-2 per million [91] Antiphospholipid syndrome: Antiphospholipid antibodies Confirmed 40-50 per 100,000 [92] Paroxysmal nocturnal hemoglobinuria: None specific, mutation causes self-cells to become susceptible to ...
In persistent left superior vena cava, the left brachiocephalic vein does not develop fully and the left upper limb and head and neck drain into the right atrium via the coronary sinus.
A 29-year-old man’s debilitating night terrors were the first sign of rare autoimmune disorder that rapidly progressed, landing him in the intensive care unit in a “catatonic state.” Ben ...
It is a rare cause of pulmonary hypertension, and occurs predominantly in young adults. [2] [3] Together with pulmonary veno-occlusive disease, PCH comprises WHO Group I' causes for pulmonary hypertension. Indeed, there is some evidence to suggest that PCH and pulmonary veno-occlusive disease are different forms of a similar disease process. [4]