Symptoms and Findings Associated with Pulmonary Vascular Disease

Oxygen saturation in high-altitude pulmonary edema

James J. Bachman, Todd Beatty, Daniel E. LeveneUniversity of Colorado.United States Journal of the American Board of Family PracticeJ Am Board Fam Prac 1992; 5: 429-431DOI: Not Available AbstractAbstract Not Available CategoryHigh Altitude Pulmonary EdemaSymptoms and Findings Associated with Pulmonary Vascular Disease Age Focus: Pediatric Pulmonary Vascular Disease or Adult Pulmonary Vascular Disease Fresh or Filed Publication: […]

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High-altitude pulmonary edema in children

Ralph C. Frates Jr, Gunyon M. Harrison, George A. EdwardsBaylor Collegeof Medicine and the Texas Institute for Rehabilitation and Research.United States American Journal of Diseases of ChildrenAm J Dis Child 1977; 131: 687-689DOI: 10.1001/archpedi.1977.02120190081018 AbstractA 15-year-old boy with recurrent high-altitude pulmonary edema had previously been mistakenly treated for asthma and pneumonia. Clinical manifestations of this disorder,

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SOX17 variants are associated with severe pulmonary arterial hypertension with and without congenital heart disease

Cara Morgan, Laura Southgate, Alistair Calder, Thivya Sekar, Andrew Constantine, Sadia Quyam, Richard Trembath, Shahin MoledinaGreat Ormond Street Hospital for Children. University of London, School of Health & Medical Sciences. Queen Elizabeth Hospital Birmingham. University College London. King’s College London. United Kingdom International Journal of CardiologyInt J Cardiol 2025; DOI: 10.1016/j.ijcard.2025.134114 AbstractBackground: SOX17 has recently been identified

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Juvenile-onset mixed connective tissue disease: A multicenter retrospective cohort study

Kevin Chevalier, Brigitte Bader-Meunier, Isabelle Kone-Paut, Benjamin Thoreau, Marc Michel, Bertrand Godeau, Christian Agard, Thomas Papo, Karim Sacre, Rapha`ele Seror, Xavier Mariette, Patrice Cacoub, Ygal Benhamou, Mathilde Leclercq, C´ecile Goujard, Olivier Lambotte, Bernard Bonnotte, Maxime Samson, Félix Ackermann, Jean Schmidt, Pierre Duhaut, Jean-Emmanuel Kahn, Thomas Hanslik, Nathalie Costedoat-Chalumeau, Benjamin Terrier, Alexis Regent, Bertrand Dunogue, Pascal

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A rare case of isolated unilateral pulmonary vein atresia presenting as interstitial lung disease in a young adult

Arnav Shandil, Mansi Verma, Sushma Makhaik, Sumala KapilaIndira Gandhi Medical CollegeIndia Journal of Cardiovascular and Thoracic ResearchJ Cardiovasc Thorac Res 2025; 17: 212-214DOI: 10.34172/jcvtr.025.33139 AbstractUnilateral pulmonary vein atresia is an unusual congenital cardiovascular abnormality. It occurs due to failure of incorporation of pulmonary veins into the left atrium. It is usually diagnosed in childhood and diagnosis

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Dermatologic findings in hereditary hemorrhagic telangiectasia: association with epistaxis, visceral involvement, and genetics

Andrea Michelerio, Giuseppe Spinozzi, Chiara Giorgini, Carla Olivieri, Annalisa de Silvestri, Fabio Pagella, Camilla VassalloUniversity of Pavia. Fondazione IRCCS Policlinico San Matteo. Italy Italian Journal of Dermatology and VenereologyItal J Dermatol Venereol 2025; DOI: 10.23736/S2784-8671.25.08225-8 AbstractBackground: Hereditary hemorrhagic telangiectasia (HHT) is a genetic vascular disorder characterized by epistaxis, mucocutaneous telangiectasias, and visceral arteriovenous malformations (AVMs). Despite the

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Pulmonary vascular complications in children who survive long-term after Kasai portoenterostomy for biliary atresia: a narrative review

Jie Zhang, Gong ChenChildren’s Hospital of Fudan University.China World Journal of Pediatric SurgeryWorld J Pediatr Surg 2025; 8: DOI: 10.1136/wjps-2025-001067 AbstractFollowing Kasai portoenterostomy for biliary atresia (BA), long-term survival in children is associated with chronic liver cirrhosis leading to hepatopulmonary syndrome (HPS) and portopulmonary hypertension (PoPH). This further causes a diverse array of respiratory and circulatory

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Pulmonary arterial hypertension increases the risk of female sexual dysfunction: a systematic review and meta-analysis

Xiaoyu. Qiao, Danyan Su, Suyuan Qin, Lifeng Shang, Liu Luo, Yusheng PangFirst Affiliated Hospital of Guangxi Medical University and Pediatric Clinical Medical Research Center of Guangxi.China Journal of Sexual MedicineJ Sex Med 2025; DOI: 10.1093/jsxmed/qdaf294 AbstractBackground: An increasing body of research has investigated the sexual functioning status in women with pulmonary arterial hypertension (PAH); yet, the evidence

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One-stage relief of bilateral outflow tract obstruction and left main coronary ostial stenosis in an infant with Williams syndrome: the technique

Ali H. Mashadi, Yasin Essa & Sameh M. SaidMaria Fareri Children’s Hospital and Westchester Medical Center.United States Multimedia Manual of Cardio-Thoracic SurgeryMultimed Man Cardiothorac Surg 2025; DOI: 10.1510/mmcts.2024.117 AbstractA 3-month-old, 5.2-kg infant with Williams syndrome presented with failure to thrive and a systolic murmur. He was taken to the cardiac catheterization laboratory for a planned pulmonary

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