The Experts below are selected from a list of 60 Experts worldwide ranked by ideXlab platform
Preethi Balan - One of the best experts on this subject based on the ideXlab platform.
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a case report of Marfans Syndrome patient with epilepsy a rare concomitance
Journal of contemporary medicine, 2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi BalanAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy.
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A case report of Marfans Syndrome patient with epilepsy-A Rare concomitance
Scopemed, 2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi BalanAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy. [J Contemp Med 2012; 2(1.000): 33-37
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a case report of Marfans Syndrome patient with epilepsy a rare concomitance epilepsi ile birlikte marfan sendromu olgu sunusu nadir bir birliktelik
2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi Balan, Shetty MemorialAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy.
Deepa Dsouza - One of the best experts on this subject based on the ideXlab platform.
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a case report of Marfans Syndrome patient with epilepsy a rare concomitance
Journal of contemporary medicine, 2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi BalanAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy.
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A case report of Marfans Syndrome patient with epilepsy-A Rare concomitance
Scopemed, 2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi BalanAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy. [J Contemp Med 2012; 2(1.000): 33-37
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a case report of Marfans Syndrome patient with epilepsy a rare concomitance epilepsi ile birlikte marfan sendromu olgu sunusu nadir bir birliktelik
2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi Balan, Shetty MemorialAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy.
Shishir Ram Shetty - One of the best experts on this subject based on the ideXlab platform.
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a case report of Marfans Syndrome patient with epilepsy a rare concomitance
Journal of contemporary medicine, 2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi BalanAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy.
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A case report of Marfans Syndrome patient with epilepsy-A Rare concomitance
Scopemed, 2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi BalanAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy. [J Contemp Med 2012; 2(1.000): 33-37
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a case report of Marfans Syndrome patient with epilepsy a rare concomitance epilepsi ile birlikte marfan sendromu olgu sunusu nadir bir birliktelik
2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi Balan, Shetty MemorialAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy.
Subhas Babu G - One of the best experts on this subject based on the ideXlab platform.
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a case report of Marfans Syndrome patient with epilepsy a rare concomitance
Journal of contemporary medicine, 2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi BalanAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy.
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A case report of Marfans Syndrome patient with epilepsy-A Rare concomitance
Scopemed, 2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi BalanAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy. [J Contemp Med 2012; 2(1.000): 33-37
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a case report of Marfans Syndrome patient with epilepsy a rare concomitance epilepsi ile birlikte marfan sendromu olgu sunusu nadir bir birliktelik
2012Co-Authors: Deepa Dsouza, Subhas Babu G, Shishir Ram Shetty, Preethi Balan, Shetty MemorialAbstract:Marfans Syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mutation in the fibrillin gene. The Syndrome has a wide range of expression from mild to the severe forms. Sometimes the symptoms are so mild that only few of the symptoms occur. In most cases, the disease progresses with age and symptoms of Marfans Syndrome become noticeable as changes in the connective tissue occur. Most of the reported cases so far are associated with cardiovascular abnormalities. We report a case of Marfans Syndrome associated with epilepsy.
Tomayoshi Hayashi - One of the best experts on this subject based on the ideXlab platform.
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risk of development of abdominal aortic aneurysm and dissection of thoracic aorta in a postpartum womanwith Marfans Syndrome
Internal Medicine, 2006Co-Authors: Aki Tomihara, Naoto Ashizawa, Kuniko Abe, Naoe Kinoshita, Keisuke Chihaya, Tsuyoshi Yonekura, Satoki Fukae, Kazuto Ashizawa, Kiyoyuki Eishi, Tomayoshi HayashiAbstract:A 24-year-old pregnant woman with Marfan’s Syndrome delivered by cesarean section during the 38th week of gestation. Although aortic root dilatation did not increase during pregnancy, three months after delivery, the patient noticed a pulsatile abdominal mass. Aortic aneurysm was diagnosed and surgical replacement of the infrarenal abdominal aorta to the common iliac arteries and reconstruction of the inferior mesenteric artery were performed. Moreover, the patient subsequently developed a Stanford type B thoracic aortic dissection, even after more than four months of β-blockade.