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Updated: Jun 29, 2025

The Left Pneumonectomy Combined with Monocrotaline or Sugen as a Model of Pulmonary Hypertension in Rats
Published on: March 8, 2019
Heritable Pulmonary Arterial Hypertension in a Patient With Empty Sella Syndrome: A Case Report
Bader Alghamdi1, Shahad Aljuhani2, Ghaday Alansari2
1Pulmonology, King Abdulaziz Medical City, Jeddah, SAU.
Abstract:
Pulmonary arterial hypertension (PAH) is a progressive disease with multiple contributing factors. Genetics, epigenetics, hormonal, and immune factors all contribute to the development and progression of the disease. A number of endocrine disorders and metabolic syndromes are being studied for their potential role in the development of PAH. We report to you a case of a 32-year-old female with a rare presentation of a non-BMPR2 mutation heritable PAH complicated with empty sella syndrome and panhypopituitarism.
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Pleiotropy