Results 61 to 70 of about 3,134 (182)

Renal Phosphate Reabsorption in Humans Depends on at Least Three Distinct Transporters Unlike in Mice

Acta Physiologica, Volume 242, Issue 8, August 2026.
ABSTRACT Aim Kidney excretion of phosphate is the gatekeeper of systemic phosphate homeostasis as evident from inborn and acquired diseases. Renal phosphate transporters are a promising target for phosphate‐lowering drugs, but molecular details of human kidney phosphate handling are largely unknown.
Ashley L. Fernandes, Laurine Lang, Jürgen Klar, Anja Giese, Alexander Ehrmann, Rupert Busch, Hannah Auwerx, Christoph Daniel, Nati Hernando, Isabel Rubio‐Aliaga, Carsten A. Wagner   +10 more
wiley   +1 more source

CONGENITAL DIAPHRAGMATIC HERNIA

Annals of Surgery, 1923
Posterolateral congenital diaphragmatic hernia (Bochdalek's hernia, CDH) that presents in the neonatal period is often manifest as life-threatening respiratory distress due to mechanical compression of the cardiopulmonary system by herniated viscera. Most patients can be supported through surgical reduction and repair with standard neonatal techniques.
J F, Connors, W T, Robinson
openaire   +3 more sources

Incidentally revealing of CHD in a 52 year-old man: Case report and literature review

Radiology Case Reports
Congenital hernia of the diaphragmatic dome is defined as a congenital embryopathy where all or part of the diaphragmatic dome fails to form during embryonic development.
Idriss Chami Khazraji, MD, Rayhana Charif Saibari, MD, Samia Bennani, MD, Amal Rami, PhD, Mohamed Amine Ait Achour, MD, Rajaa Lafhal, MD, Mustapha Noussair, PhD   +6 more
doaj   +1 more source

Living Donor Liver Transplantation in Pediatric Situs Inversus: A Case Series and Systematic Review

Pediatric Transplantation, Volume 30, Issue 8, August 2026.
ABSTRACT Liver transplantation (LT) in patients with situs inversus (S‐I) is rare and technically challenging. The literature on such cases, particularly in pediatric populations, remains limited. Here, we report the surgical considerations and outcomes of two pediatric recipients with situs inversus abdominalis who underwent liver transplantation for ...
Maria F. Fernandez, Nadia Ali, Carolina Rumbo, Piyush Gupta, Kathryn LaRusso, Nada Yazigi, Christof Kaltenmeier, Juan F. Guerra, Leonardo A. Montes, Udeme Ekong, Alexander Kroemer, Dolores Garcia‐Hervas, Khalid Khan, Yuri Genyk, Cal Matsumoto, Julio Trentadue, Diego Ramisch, Pablo Barros‐Schelotto, Thomas Fishbein, Gabriel E. Gondolesi   +19 more
wiley   +1 more source

Laparoscopic Repair of Morgagni Hernia

Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2015
Morgagni hernia is a congenital herniation of abdominal contents into the thoracic cavity through a retrosternal diaphragmatic defect and make up about 1 % - 5 % of all types of congenital diaphragmatic hernias.
ilker murat arer, Hakan Yabanoglu, huseyin ozgur aytac, Kenan Caliskan, nurkan torer   +4 more
doaj  

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Clinical Presentations and Surgical Features of Morgagni Hernia in Adults: A Retrospective Study

Health Science Reports
Background and Aims Morgagni hernias are rare congenital diaphragmatic defects that can lead to bowel obstruction and incarceration if not repaired. While this disease typically manifests as respiratory distress, frequent respiratory infections, and ...
Parviz Mardani, Farzad Dalfardi, Saman Bahmani, Rahem Rahmati, Fatemeh Zarimeidani, Bizhan Ziaian, Armin Amirian, Masoud Vafabin, Reza Shahriarirad   +8 more
doaj   +1 more source

Atypical right diaphragmatic hernia (hernia of Morgagni), spigelian hernia and epigastric hernia in a patient with Williams syndrome: a case report

Journal of Medical Case Reports, 2009
Introduction Williams syndrome is rare genetic disorder resulting in neurodevelopmental problems. Hernias of the foramen of Morgagni are rare diaphragmatic hernias and they mostly present on the right side, in the anterior mediastinum.
Rashid Farhan, Chaparala Ramakrishna, Ahmed Javed, Iftikhar Syed Y   +3 more
doaj   +1 more source

Late presentation of congenital diaphragmatic hernia: A diagnostic dilemma

Bangabandhu Sheikh Mujib Medical University Journal, 2016
Congenital diaphragmatic hernias are commonly symptomatic within 24 hours after birth, but late presentation is not uncommon. Late presentation of congenital diaphragmatic hernia poses diagnostic difficulties as clinical picture are vague, and more ...
Dinesh Gurung, Shanker Bhandari, Md. Aftabuddin, Asit Baran Adhikary   +3 more
doaj   +1 more source

Laparoscopic transabdominal Morgagni hernia repair

International Journal of Abdominal Wall and Hernia Surgery, 2018
Morgagni hernias are a rare finding in the adult population and represent 1%–3% of all congenital diaphragmatic hernias. Multiple approaches to these rare hernias have been described in the literature.
Rebekah Macfie, Sean Orenstein, David Tse   +2 more
doaj   +1 more source