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Quoted phrase not found in phrase index: "Congenital heart defects, multiple types, 8, with or without heterotaxy"
Page 1
Motile ciliopathies.
Wallmeier J, Nielsen KG, Kuehni CE, Lucas JS, Leigh MW, Zariwala MA, Omran H. Wallmeier J, et al. Nat Rev Dis Primers. 2020 Sep 17;6(1):77. doi: 10.1038/s41572-020-0209-6. Nat Rev Dis Primers. 2020. PMID: 32943623 Review.
The pathogenetic mechanisms, clinical symptoms and severity of the disease depend on the specific affected genes and the tissues in which they are expressed. Defects in the ependymal cilia can result in hydrocephalus, defects in the cilia in the fallopian tubes or i …
The pathogenetic mechanisms, clinical symptoms and severity of the disease depend on the specific affected genes and the tissues in which th …
Neonatal cardiovascular physiology.
Hines MH. Hines MH. Semin Pediatr Surg. 2013 Nov;22(4):174-8. doi: 10.1053/j.sempedsurg.2013.10.004. Epub 2013 Oct 14. Semin Pediatr Surg. 2013. PMID: 24331090 Review.
The pediatric surgeon deals with a large number and variety of congenital defects in neonates that frequently involve early surgical intervention and care. ...Finally, the pediatric surgeon is often called upon to treat conditions and complications associated with c …
The pediatric surgeon deals with a large number and variety of congenital defects in neonates that frequently involve early su …
Congenital Heart Disease and Primary Ciliary Dyskinesia.
Harrison MJ, Shapiro AJ, Kennedy MP. Harrison MJ, et al. Paediatr Respir Rev. 2016 Mar;18:25-32. doi: 10.1016/j.prrv.2015.09.003. Epub 2015 Sep 26. Paediatr Respir Rev. 2016. PMID: 26545972 Review.
Through the better understanding of the genetics and clinical associations of Primary Ciliary Dyskinesia (PCD), an autosomal recessive disorder of ciliary motility and mucociliary clearance, the association between PCD and heterotaxic congenital heart disease (CHD) …
Through the better understanding of the genetics and clinical associations of Primary Ciliary Dyskinesia (PCD), an autosomal recessive disor …
Intestinal Rotation Anomalies.
Pelayo JC, Lo A. Pelayo JC, et al. Pediatr Ann. 2016 Jul 1;45(7):e247-50. doi: 10.3928/00904481-20160602-01. Pediatr Ann. 2016. PMID: 27403672
Populations in which IRA is always associated, but a Ladd's procedure rarely required, include patients with congenital diaphragmatic hernia and abdominal wall defects. Prevalence of IRA is higher in children with congenital heart disease and hetero …
Populations in which IRA is always associated, but a Ladd's procedure rarely required, include patients with congenital diaphragmatic …
Congenital heart defects in Kabuki syndrome.
Yuan SM. Yuan SM. Cardiol J. 2013;20(2):121-4. doi: 10.5603/CJ.2013.0023. Cardiol J. 2013. PMID: 23558868 Free article. Review.
Congenital heart defects are one of the clinical manifestations of KS with insufficient elucidations. ...Fifteen (19.7%) patients received surgical repair of congenital heart defects at a mean age of 0.8 1.3 years. CONCLUSIONS: …
Congenital heart defects are one of the clinical manifestations of KS with insufficient elucidations. ...Fifteen (19.7% …
Bacteremia in Patients with Heterotaxy: A Review and Implications for Management.
Loomba RS, Geddes GC, Basel D, Benson DW, Leuthner SR, Hehir DA, Ghanayem N, Shillingford AJ. Loomba RS, et al. Congenit Heart Dis. 2016 Dec;11(6):537-547. doi: 10.1111/chd.12395. Epub 2016 Jul 18. Congenit Heart Dis. 2016. PMID: 27425254 Review.
Heterotaxy (HTX) is a laterality defect resulting in abnormal arrangement of the thoracic and abdominal organs across the right-left axis, and is associated with multiple anatomic and physiologic disruptions. HTX often occurs in association with complex congenita …
Heterotaxy (HTX) is a laterality defect resulting in abnormal arrangement of the thoracic and abdominal organs across the right-left …
A multi-disciplinary, comprehensive approach to management of children with heterotaxy.
Saba TG, Geddes GC, Ware SM, Schidlow DN, Del Nido PJ, Rubalcava NS, Gadepalli SK, Stillwell T, Griffiths A, Bennett Murphy LM, Barber AT, Leigh MW, Sabin N, Shapiro AJ. Saba TG, et al. Orphanet J Rare Dis. 2022 Sep 9;17(1):351. doi: 10.1186/s13023-022-02515-2. Orphanet J Rare Dis. 2022. PMID: 36085154 Free PMC article. Review.
Heterotaxy (HTX) is a rare condition of abnormal thoraco-abdominal organ arrangement across the left-right axis of the body. ...It can be inherited as a single-gene disorder, a phenotypic feature of a known genetic syndrome or without any clear genetic etiology. Mos …
Heterotaxy (HTX) is a rare condition of abnormal thoraco-abdominal organ arrangement across the left-right axis of the body. ...It ca …
Diagnosis and management of intestinal rotational abnormalities with or without volvulus in the pediatric population.
Svetanoff WJ, Srivatsa S, Diefenbach K, Nwomeh BC. Svetanoff WJ, et al. Semin Pediatr Surg. 2022 Feb;31(1):151141. doi: 10.1016/j.sempedsurg.2022.151141. Epub 2022 Feb 18. Semin Pediatr Surg. 2022. PMID: 35305800 Review.
Intestinal malrotation is a congenital anomaly that can be associated with midgut volvulus, requiring an emergent operation in order to maintain blood supply to the compromised intestine. ...Laparoscopic Ladd's is associated with shorter hospital stays but also has a highe …
Intestinal malrotation is a congenital anomaly that can be associated with midgut volvulus, requiring an emergent operation in order …
Outcomes in adults with congenital heart disease and heterotaxy syndrome: A single-center experience.
Broda CR, Salciccioli KB, Lopez KN, Ermis PR, Moodie DS, Dickerson HA. Broda CR, et al. Congenit Heart Dis. 2019 Nov;14(6):885-894. doi: 10.1111/chd.12856. Epub 2019 Oct 16. Congenit Heart Dis. 2019. PMID: 31617655 Free PMC article.
BACKGROUND: Heterotaxy syndrome (HS) is a condition in which the thoracoabdominal organs demonstrate an abnormal lateral arrangement and is often associated with congenital heart disease (CHD). ...Heart failure-free survival was 80.8 5.2% …
BACKGROUND: Heterotaxy syndrome (HS) is a condition in which the thoracoabdominal organs demonstrate an abnormal lateral arran …
Perinatal outcome in fetuses with heterotaxy syndrome and atrioventricular block or bradycardia.
Escobar-Diaz MC, Tworetzky W, Friedman K, Lafranchi T, Fynn-Thompson F, Alexander ME, Mah DY. Escobar-Diaz MC, et al. Pediatr Cardiol. 2014 Aug;35(6):906-13. doi: 10.1007/s00246-014-0874-x. Epub 2014 Feb 9. Pediatr Cardiol. 2014. PMID: 24509635 Free PMC article.
Congenital atrioventricular (AV) block is commonly associated with heterotaxy syndrome; together they have reportedly low survival rates (10-25%). ...The primary outcome was death and the secondary outcome was pacemaker placement. Of the 154 fetuses with h …
Congenital atrioventricular (AV) block is commonly associated with heterotaxy syndrome; together they have reportedly l …
520 results