Middle aortic coarctation is a rare vascular anomaly characterized by the segmental narrowing of the abdominal and/or distal descending thoracic aorta with. COARCTAŢIA DE AORTĂ, METODE DE DIAGNOSTIC ŞI TRATAMENT CONTEMPORAN. Sorbală, Tatiana. URI: Abstract Coarctation of the aorta is a congenital cardiac malformation that can go undiagnosed until old age with only hypertension as a marker of its presence.

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Loading Stack – 0 images remaining. The incidence of coarctation of the aorta is 4 in Case 19 Case Case 10 Case Late hypertension does also seem to be much less of a problem if the coarctation repair was performed not later than within the 5 first tear of life.

Unfortunately, coarctations can not be prevented because they are usually present at birth. Definition MSH A birth defect characterized by the narrowing of the AORTA that can be of varying degree and at any point from the transverse arch to the iliac ed.

Although access to this website is not restricted, the information found here is intended for use by medical providers. Arterial hypertension in the arms with low blood pressure in the lower extremities is classic.

As with many congenital abnormalities, coarctation of the aorta is associated with other congenital anomalies.


In cases of more severe coarctations, babies may develop serious problems soon after birth because coarxtacao enough blood can get through the aorta to the rest of their body. Coarctation of the aorta can be accurately diagnosed with magnetic resonance angiography.

Aortic CoarctationCoarctation of the Aorta. Journal of Cardiac Surgery.

Coarctation of the aorta

Nienaber CA, Fattori R. Related Topics in Pediatrics. Case 13 Case Thank you for updating your details. In dit proefschrift komt o.

Coarctatia de aorta | Theracardia BRASOV

They may experience dizziness or shortness of breath, fainting or near-fainting episodes, chest pain, abnormal tiredness or fatigue, headaches, or nosebleeds. Case 11 Case The documents contained in this web site are presented for information purposes only.

Long-term follow-up and prediction of outcome after surgical correction”. Many years after the procedure is done, heart disease not only has an increased chance of affecting coarctation patients, but also progresses through the levels of severity at an alarmingly increased rate. Coarctaco treatment of native aortic coarctation in adults.

From Wikipedia, the free encyclopedia. Signs and symptoms include hypertension, muscle weakness, shortness of breath, headaches and leg cramps. It may be due to various congenital or acquired causes, but it is most often secondary to an acquired inflammatory disease i. Unable to process the form. This spectrum is dichotomized by the idea that aortic coarctation occurs in the aortic arch, at or near the ductus arteriosis, whereas aortic stenosis occurs in the aortic root, at or near the aortic valve.


Coaarctacao coarctation using different imaging techniques [12]. Aanvullend wordt gekeken naar de huidige beschikbare therapeutische mogelijkheden ten aanzien van het cardiovasculair risico. About Blog Go ad-free.

Subclavian angioplasty does not reduce the need for reoperation”. Synonyms or Alternate Spellings: We report the case of a 45 year-old women, diagnosed with severe coarctation of the aorta just distal to the left subclavian artery, with poststenotic dilatation of the descending aorta and difficult control of blood pressure values. In mild cases, children may show no signs or symptoms at first and their condition may not be diagnosed until later in life.

On the other hand, a coarctation occurring after the left subclavian artery will d synchronous radial pulses, but radio-femoral delay will be present under palpation in aprta arm both arm pulses are normal aoeta to the delayed leg pulses. Case 15 Case Not to be confused with aortic stenosis. Specialised Social Services Eurordis directory. Patent ductus arteriosus Coarctation of the aorta Interrupted aortic arch Double aortic arch Right-sided aortic arch Overriding aorta Aneurysm of sinus of Valsalva Vascular ring.