Hereditary haemorrhagic telangiectasia: a rare cause of hepatic encephalopathy

HIGHLIGHTS

• who: Hereditary haemorrhagic telangiectasia and colleagues from the Advanced Trainee in Intensive Care Medicine, Liverpool Hospital, Australia have published the research: Hereditary Haemorrhagic Telangiectasia: A rare cause of Hepatic Encephalopathy, in the Journal: (JOURNAL)

SUMMARY

Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant vascular disorder that affects 1 in 50008000 individuals. The formation of AVMs occurs most frequently in the pulmonary, hepatic and cerebral circulations, with a smaller proportion developing in the spinal cord vasculature. The diagnosis of J Anest and amp; Inten Care Med 10(2): JAICM.MS.ID.555784 hepatic involvement . . .

 



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