scholarly journals Pulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardia

2019 ◽  
Vol 4 (4) ◽  
pp. 134-135
Author(s):  
Ganganpalli Dattaprasad ◽  
Umesh Kumar Chandra ◽  
Sumit K umar Vishwakarma ◽  
V.P. Pandey ◽  
Sanjay Dubey
2014 ◽  
Vol 4 (2) ◽  
pp. 342-345 ◽  
Author(s):  
Dhruv Nayyar ◽  
Kavitha Muthiah ◽  
Gayathri Kumarasinghe ◽  
Ravin Hettiarachchi ◽  
David Celermajer ◽  
...  

ESC CardioMed ◽  
2018 ◽  
pp. 2558-2560
Author(s):  
Barbara Girerd ◽  
David Montani ◽  
Marc Humbert

Pre-capillary pulmonary hypertension can be heritable in the context of pulmonary arterial hypertension (an autosomal dominant disease mainly due to mutations in BMPR2), and pulmonary veno-occlusive disease or pulmonary capillary haemangiomatosis (an autosomal recessive disease due to biallelic mutations in the EIF2AK4 gene). Genetic counselling can be implemented in referral centres for pulmonary hypertension as outlined in this chapter.


ESC CardioMed ◽  
2018 ◽  
pp. 2558-2560
Author(s):  
Barbara Girerd ◽  
David Montani ◽  
Marc Humbert

Pre-capillary pulmonary hypertension can be heritable in the context of pulmonary arterial hypertension (an autosomal dominant disease mainly due to mutations in BMPR2), and pulmonary veno-occlusive disease or pulmonary capillary haemangiomatosis (an autosomal recessive disease due to biallelic mutations in the EIF2AK4 gene). Genetic counselling can be implemented in referral centres for pulmonary hypertension as outlined in this chapter.


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