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SMA syndrome is also known as Wilkie's syndrome, cast syndrome, mesenteric root syndrome, chronic duodenal ileus and intermittent arterio-mesenteric occlusion. [3] It is distinct from nutcracker syndrome , which is the entrapment of the left renal vein between the AA and the SMA, although it is possible to be diagnosed with both conditions.
The management of isolated superior mesenteric artery dissection (ISMAD) often involves conservative treatment, which includes blood pressure lowering therapy, analgesics, and initial bowel rest. [4] Periodic follow-ups with CT angiography are a part of the conservative treatment approach. Over time, many patients show improvement or no change ...
Treatment Supportive Care Spinal and bulbar muscular atrophy ( SBMA ), popularly known as Kennedy's disease , is a rare, adult-onset, X-linked recessive lower motor neuron disease caused by trinucleotide CAG repeat expansions in exon 1 of the androgen receptor (AR) gene, which results in both loss of AR function and toxic gain of function.
Spinal muscular atrophy, or SMA, was the leading cause of genetic deaths in babies, but screenings and new treatments are now helping kids thrive. Spinal muscular atrophy, or SMA, was the leading ...
Spinal muscular atrophy (SMA) is a rare neuromuscular disorder that results in the loss of motor neurons and progressive muscle wasting. [ 3 ] [ 4 ] [ 5 ] It is usually diagnosed in infancy or early childhood and if left untreated it is the most common genetic cause of infant death. [ 6 ]
Abdominal angina is caused by obstruction or stenosis of the inferior mesenteric artery, celiac trunk, or superior mesenteric artery. Gender, age, smoking, hypertension, diabetes, and hyperlipidemia are risk factors for abdominal angina. The digestive tract relies on the celiac, superior mesenteric, and inferior mesenteric arteries for blood ...
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