Neonatal Marfan syndrome diagnosed prenatally
نویسندگان
چکیده
منابع مشابه
Neonatal outcomes of prenatally diagnosed congenital pulmonary malformations.
BACKGROUND AND OBJECTIVE Congenital pulmonary malformations (CPM) are mostly recognized on prenatal ultrasound scans. In a minority of cases, they may impair breathing at birth. The factors predictive of neonatal respiratory distress are not well defined, but an understanding of these factors is essential for decisions concerning the need for the delivery to take place in a tertiary care center...
متن کاملNeonatal Marfan syndrome: a case report.
A case of neonatal Marfan syndrome is presented. The patient was noted to have cardiomegaly and tricuspid regurgitation on antenatal ultrasound scan. She was born with long, slender fingers and toes, an aged appearance and non-paralytic hypotonia. Echocardiogram revealed a dilated right atrium, right ventricle, dysplastic tricuspid valve and severe tricuspid regurgitation. She subsequently died...
متن کاملNeonatal Marfan Syndrome: Report of Two Cases
Marfan syndrome is rarely diagnosed in the neonatal period because of variable expression and age-dependent appearance of clinical signs. The prognosis is usually poor due to high probability of congestive heart failure, mitral and tricuspid regurgitations with suboptimal response to medical therapy and difficulties in surgical management. The authors have studied two cases of Marfan syndrome i...
متن کاملMarfan Syndrome With Bicuspid Aortic Valve Diagnosed By Transesophageal Echocardiography
In diagnosing MS, even though investigators recently identified a defective FBN 1 gene as cause of this hereditary condition, employing a genetic test a sa diagnostic tool is not partical in the near future (3). This is because of the extreme variability in the FBN 1 gene on chromosome 15. It has been shown (1) that transesophageal echocardiography (TEE) provides rapid diagnostic information in...
متن کاملIncreased homocysteine in a patient diagnosed with Marfan syndrome.
A 53-year-old Caucasian woman was diagnosed in late childhood with Marfan syndrome according to characteristic skeletal features and bilateral lens dislocation. In addition, she has a history of nonischemic cardiomyopathy with severe left ventricular failure and atrial fibrillation, diabetes mellitus type 2, hyperlipidemia, progressive dementia, numbness in the lower extremities, and hypothyroi...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Ginekologia Polska
سال: 2017
ISSN: 2543-6767,0017-0011
DOI: 10.5603/gp.a2017.0009