Health / Medical Topics |
Septo-Optic Dysplasia
A very rare congenital syndrome characterized by hypoplasia of the optic nerve, impaired vision, absence of the septum pellucidum and hypopituitarism. (NCI Thesaurus)
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Septin-9 (586 aa, ~65 kDa) is encoded by the human SEPT9 gene. This protein plays a role in the mediation of cytoskeletal…
Septin-6 (434 aa, ~50 kDa) is encoded by the human SEPT6 gene. This protein is involved in cytokinesis.
Septin-5 (369 aa, ~43 kDa) is encoded by the human SEPT5 gene. This protein plays a role in cytokinesis.
Septin-4 (478 aa, ~55 kDa) is encoded by the human SEPT4 gene. This protein is involved in both cytoskeletal structure and GTP…
Disease caused by the spread of bacteria and their toxins in the bloodstream. Also called blood poisoning and toxemia.
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