Heritable Pulmonary Arterial Hypertension in a Patient With Empty Sella Syndrome: A Case Report

被引：0
|
作者：
Alghamdi, Bader [1 ]
Aljuhani, Shahad [2 ]
Alansari, Ghaday [2 ]
Binhumaid, Nouf M. [3 ]
Alkahtani, Abdulkareem [2 ,4 ]
机构：
[1] King Abdul Aziz Med City, Pulmonol, Jeddah, Saudi Arabia
[2] King Saud Bin Abdulaziz Univ Hlth Sci, Coll Med, Jeddah, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Pulmonol, Jeddah, Saudi Arabia
[4] King Abdul Aziz Med City, Med Imaging, Jeddah, Saudi Arabia
来源：
CUREUS JOURNAL OF MEDICAL SCIENCE | 2024年 / 16卷 / 02期
关键词：
non-bmpr2; heritable pah; genetics; empty sella syndrome; pulmonary arterial hypertension;
D O I：
10.7759/cureus.54632
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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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页数：5
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