Page last updated: 2024-11-07

aldosterone and Marfan Syndrome

aldosterone has been researched along with Marfan Syndrome in 1 studies

Marfan Syndrome: An autosomal dominant disorder of CONNECTIVE TISSUE with abnormal features in the heart, the eye, and the skeleton. Cardiovascular manifestations include MITRAL VALVE PROLAPSE, dilation of the AORTA, and aortic dissection. Other features include lens displacement (ectopia lentis), disproportioned long limbs and enlarged DURA MATER (dural ectasia). Marfan syndrome (type 1) is associated with mutations in the gene encoding FIBRILLIN-1 (FBN1), a major element of extracellular microfibrils of connective tissue. Mutations in the gene encoding TYPE II TGF-BETA RECEPTOR (TGFBR2) are associated with Marfan syndrome type 2.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Takeda, R1
Morimoto, S1
Kuroda, M1
Murakami, M1

Other Studies

1 other study available for aldosterone and Marfan Syndrome

ArticleYear
Renal tubular acidosis, presenting as a syndrome resembling Bartter's syndrome, in a patient with arachnodactyly.
    Acta endocrinologica, 1973, Volume: 73, Issue:3

    Topics: Acidosis, Renal Tubular; Adult; Aldosterone; Alkalosis; Biopsy; Humans; Hyperaldosteronism; Hyperpla

1973