Zobrazeno 1 - 10
of 220
pro vyhledávání: '"hypoplastic lung"'
Publikováno v:
Lung India, Vol 38, Iss 1, Pp 86-87 (2021)
Congenital isolated unilateral hypoplasia of the pulmonary artery (CIUPAH) can have late presentation in the adulthood, mostly diagnosed incidentally, as in our case. They may have symptoms such as exertional dyspnea, recurrent lung infections, and h
Externí odkaz:
https://doaj.org/article/1b97dbc89e484e70a806b5f515fe5531
Autor:
Sriharsha Bokka, Ashwin Ashok Jaiswal, Bikram K Behera, Manoj Kumar Mohanty, Manish K Khare, Amrish Kumar Garg
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 20, Iss 2, Pp 92-94 (2015)
A 2-year-old female child was referred from a private hospital as a case of recurrent lower respiratory tract infections (LRTI). The chest X ray revealed a hypoplastic right lung and further workup led to the diagnosis of esophageal lung - a rare typ
Externí odkaz:
https://doaj.org/article/9a14a4bf96c14086824e4e8e941385ed
Autor:
Oluyinka O. Olutoye II, Walker D. Short, Jamie Gilley, J. D. Hammond II, Michael A. Belfort, Timothy C. Lee, Alice King, Jimmy Espinoza, Luc Joyeux, Krithika Lingappan, Jason P. Gleghorn, Sundeep G. Keswani
Publikováno v:
Frontiers in pediatrics. 10
Congenital diaphragmatic hernia (CDH) is a complex disease associated with pulmonary hypoplasia and pulmonary hypertension. Great strides have been made in our ability to care for CDH patients, specifically in the prenatal improvement of lung volume
Publikováno v:
Clinical Case Reports, Vol 8, Iss 9, Pp 1698-1703 (2020)
Clinical Case Reports
Clinical Case Reports
Unilateral pulmonary vein atresia (UPVA) is a rare congenital vascular malformation with obliteration of the pulmonary vein. We present a case series of three siblings with variable presentation of UPVA. We suggest a dominant genetic cause based on d
Publikováno v:
Asian Journal of Surgery, Vol 29, Iss 1, Pp 31-35 (2006)
We performed a urinary tract obstruction (UTO) surgical procedure at 93-107 days' gestation in lambs to investigate the relationship between pulmonary hypoplasia and the appearance of pulmonary endocrine cells by quantitative analysis of respiratory
Externí odkaz:
https://doaj.org/article/93f5e434c19146b09e4302520d8be53d
Autor:
Jan Deprest, Erin E. Perrone
Publikováno v:
Transl Pediatr
Fetal intervention for fetuses with congenital diaphragmatic hernia (CDH) has been investigated for over 30 years and is summarized in this manuscript. The review begins with a discussion of the history of fetal intervention for this severe congenita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbdae98b35f9df01af8b67c4d873c621
https://lirias.kuleuven.be/handle/20.500.12942/700742
https://lirias.kuleuven.be/handle/20.500.12942/700742
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 64(1)
Publikováno v:
Brazilian Journal of Cardiovascular Surgery
Brazilian Journal of Cardiovascular Surgery, Vol 36, Iss 1, Pp 133-136 (2020)
Brazilian Journal of Cardiovascular Surgery, Vol 36, Iss 1, Pp 133-136 (2020)
Infantile scimitar syndrome (SS) is a rare congenital heart disease and has high mortality. Guidelines have not been established, but surgery is indicated in symptomatic patients. Despite the various surgical approaches, outcomes continue to be disap
Autor:
Makoto Noguchi, Shuichi Imaue, Hidetake Tachinami, Kumiko Fujiwara, Kei Tomihara, Katsuhisa Sekido
Publikováno v:
Oral Science International. 15:36-39
Scimitar syndrome is a rare congenital cardiac condition with a poor prognosis. It is frequently accompanied by concordant pulmonary hypoplasia and aortopulmonary collateral arteries connected to the hypoplastic lung. Here we report a case involving
Publikováno v:
Chest. 160:A1968