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The Intersection of Genes and Environment: Development of Pulmonary Arterial Hypertension in a Patient With Hereditary Hemorrhagic Telangiectasia and Stimulant Exposure

Pulmonary arterial hypertension (PAH) is a rare complication of hereditary hemorrhagic telangiectasia (HHT). The triggers that promote the development of PAH in HHT remain poorly understood. We present the case of a 45-year-old woman with decompensated right-sided heart failure secondary to newly di...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Ayala, Estela, Kudelko, Kristina T., Haddad, Francois, Zamanian, Roham T., de Jesus Perez, Vinicio
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American College of Chest Physicians 2012
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3367481/
https://ncbi.nlm.nih.gov/pubmed/22670022
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1378/chest.11-1402
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