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Pulmonary microvascular architecture in hereditary haemorrhagic telangiectasia

Maximilian Ackermann1, Steven J Mentzer2, Wilfried Roth3

  • 1Institute of Functional and Clinical Anatomy, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Thorax
|January 4, 2017
PubMed
Abstract

No abstract available in PubMed .

Keywords:
Histology/CytologyImaging/CT MRI etcRare lung diseases

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Pulmonary Hypertension: Classification and Pathogenesis01:30

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Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
There are various classifications for PH, each relating to different underlying causes and also...
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