| Health / Medical Topics |
Loeys-Dietz Syndrome Type 1
A rare autosomal dominant syndrome caused by mutations in the TGFBR1 gene. It is characterized by vascular abnormalities (aortic and arterial aneurysms, aortic dissection, and tortuosity of the arteries), hypertelorism, bifid uvula, and early fusion of the skull bones. (NCI Thesaurus)
YOU MAY ALSO LIKE
A rare autosomal dominant syndrome caused by mutations in the TGFBR1 or TGFBR2 genes. It is characterized by vascular abnormalities including aortic…
A wind-deposited sediment consisting mostly of silt, the silt commonly derived from finely ground rock washed out of continental glaciers. …
The tromethamide salt form of lodoxamide, a synthetic mast cell stabilizing compound with anti-inflammatory activity. Upon administration to the eye, lodoxamide tromethamide…
A synthetic mast cell stabilizing compound with anti-inflammatory activity. Lodoxamide appears to inhibit the antigen-stimulated calcium transport across the mast cell membrane,…
A synthetic purine fluoro-dideoxyadenosine derivative, antiviral Lodenosine acts as a reverse transcriptase inhibitor. Although used in clinical trials for treatment of human…
The total relative probability, expressed on a logarithmic scale, that a linkage relationship exists among selected loci. LOD is an acronym for…
