fibromuscular वाक्य
उदाहरण वाक्य
मोबाइल
- He was born with fibromuscular disproportion, a condition that led to uneven muscle development.
- It consists of a single fibromuscular structure with several layers that are fused together and covering the seminal vesicles.
- Other abnormalities to the blood vessels, such as fibromuscular dysplasia, have been reported in a proportion of cases.
- In most people fibromuscular dysplasia or atherosclerosis is the reason for the occlusion of a renal artery which ultimately leads to this condition.
- Patients with Down syndrome, sickle cell anemia, neurofibromatosis type 1, congenital heart disease, fibromuscular dysplasia, activated protein C resistance, or head trauma can develop moyamoya malformations.
- Histologically, they are outpouchings of gallbladder mucosa into the gallbladder muscle layer and subserosal tissue as a result of hyperplasia and herniation of epithelial cells through the fibromuscular layer of the gallbladder wall.
- Further episodes of cervical artery dissection are more common in those who are younger, have a family history of cervical artery dissection, or have a diagnosis of Ehlers-Danlos syndrome or fibromuscular dysplasia.
- Thoracic outlet obstruction may be caused by a number of abnormalities, including degenerative or bony disorders, trauma to the cervical spine, fibromuscular bands, vascular abnormalities, and spasm of the anterior scalene muscle.
- "' Ex vivo reconstruction "', short for ex vivo renal artery reconstruction and autotransplantation, is a technique mainly used for complex disease involving multiple segmental branches in patients with fibromuscular dysplasia.
- Between the termination of the vertebral column and the anus, the two pubococcygei muscles come together and form a thick, fibromuscular layer lying on the raphe ( ridge ) or ( anococcygeal body ) formed by the iliococcygei.
- Observational studies and case reports published since the early 1980s show that patients with spontaneous internal carotid artery dissection may also have a history of stroke in their family and / or hereditary connective tissue disorders, such as Marfan syndrome, Ehlers-Danlos syndrome, autosomal dominant polycystic kidney disease, pseudoxanthoma elasticum, fibromuscular dysplasia, and osteogenesis imperfecta type I . IgG4-related disease involving the carotid artery has also been observed as a cause.
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