| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Annalisa Chiodi, Maria Escolino, Claudia Di Mento, Vincenzo Salvati, Valerio Mazzone, Giorgia Esposito, Mauro Porcaro, Ciro Esposit. Unusual late-onset hypertrophic pyloric stenosis in an adolescent girl with down syndrome: Case report and review of the literature. Journal of clinical ultrasound : JCU. 2024-08-03. PMID:39096100. |
unusual late-onset hypertrophic pyloric stenosis in an adolescent girl with down syndrome: case report and review of the literature. |
2024-08-03 |
2024-08-06 |
Not clear |
| Carmine Noviello, Mercedes Romano, Letizia Trotta, Giuseppina Rosaria Umano, Alfonso Papparell. Are the complications after laparo-assisted endo-rectal pull-through for Hirschsprung disease related to the change of the anal tone? La Pediatria medica e chirurgica : Medical and surgical pediatrics. vol 46. issue 2. 2024-07-04. PMID:38963345. |
nine related pathologies were identified: five cases of down syndrome, one case of hypertrophic stenosis of the pylorus, atresia of the esophagus, polydactyly, and anorectal malformation. |
2024-07-04 |
2024-07-10 |
Not clear |
| Bassem Al Hariri, Muad Abdi Hassan, Muhammad Sharif, Rawan S Mohamed, Hadil Altaj Altrify Alsidig, Hind Altag Alteraify Alsiddig, Memon Noor Illah. An idiopathic severe macroglossia in a young adult patient: a rare case. Journal of surgical case reports. vol 2024. issue 5. 2024-05-21. PMID:38764739. |
congenital macroglossia stems from diverse conditions, such as muscular hypertrophy, hemangioma, lymphangioma, down syndrome, and others. |
2024-05-21 |
2024-05-27 |
Not clear |
| Rajiv R Iyer, Douglas L Brockmeye. C1 hypertrophic lateral mass resection and occiput-C2 fusion. Neurosurgical focus: Video. vol 3. issue 1. 2022-10-26. PMID:36285116. |
this case involved a 6-year-old boy with down syndrome, left c1 lateral mass hypertrophy, c1-2 rotatory subluxation, and spinal cord compression. |
2022-10-26 |
2023-08-14 |
Not clear |
| Yue Xu, Boyu Yang, Yaguang Hu, Lin Lu, Xi Lu, Jiawei Wang, Qinmeng Shu, Qiaochu Cheng, Shanshan Yu, Fan Xu, Jingjing Huang, Xiaoling Lian. Secretion of Down Syndrome Critical Region 1 Isoform 4 in Ischemic Retinal Ganglion Cells Displays Anti-Angiogenic Properties Via NFATc1-Dependent Pathway. Molecular neurobiology. vol 54. issue 8. 2018-07-09. PMID:27734335. |
down syndrome candidate region 1 (dscr1) has two differentially regulated isoforms (dscr1-1 and dscr1-4) and is reported to play a role in a number of physiological processes, such as the inhibition of cardiac hypertrophy, attenuation of angiogenesis and carcinogenesis, and protection against neuronal death. |
2018-07-09 |
2023-08-13 |
mouse |
| J Drew Prosser, Sally R Shott, Oscar Rodriguez, Narong Simakajornboon, Jareen Meinzen-Derr, Stacey L Ishma. Polysomnographic outcomes following lingual tonsillectomy for persistent obstructive sleep apnea in down syndrome. The Laryngoscope. vol 127. issue 2. 2017-08-18. PMID:27515709. |
lingual tonsil hypertrophy is a common cause of persistent airway obstruction in patients with down syndrome (ds) following adenotonsillectomy (t&a); however, little is known about the effect of lingual tonsillectomy (lt) on polysomnographic outcomes in these patients. |
2017-08-18 |
2023-08-13 |
Not clear |
| Guruprasad Mahadevaiah, Manoj Gupta, Ravi Ashwat. Down Syndrome with Complete Atrioventricular Septal Defect, Hypertrophic Cardiomyopathy, and Pulmonary Vein Stenosis. Texas Heart Institute journal. vol 42. issue 5. 2016-08-10. PMID:26504441. |
down syndrome with complete atrioventricular septal defect, hypertrophic cardiomyopathy, and pulmonary vein stenosis. |
2016-08-10 |
2023-08-13 |
Not clear |
| Guruprasad Mahadevaiah, Manoj Gupta, Ravi Ashwat. Down Syndrome with Complete Atrioventricular Septal Defect, Hypertrophic Cardiomyopathy, and Pulmonary Vein Stenosis. Texas Heart Institute journal. vol 42. issue 5. 2016-08-10. PMID:26504441. |
we found only one reported case of congenital hypertrophic cardiomyopathy and atrioventricular septal defect in an infant with down syndrome. |
2016-08-10 |
2023-08-13 |
Not clear |
| Francesca Galluzzi, Lorenzo Pignataro, Renato Maria Gaini, Werner Garavell. Drug induced sleep endoscopy in the decision-making process of children with obstructive sleep apnea. Sleep medicine. vol 16. issue 3. 2015-12-18. PMID:25754384. |
in children with down syndrome, the combined estimated rate of hypertrophic tonsils and/or adenoids was 62% (95%ci: 44-79%). |
2015-12-18 |
2023-08-13 |
Not clear |
| Laxmi Ghimire, Ossama Tawffik, Valerie A Schroede. Combined obstructive hypertrophic cardiomyopathy and double outlet right ventricle in an infant with Down syndrome. The American journal of case reports. vol 14. 2013-11-13. PMID:24222815. |
combined obstructive hypertrophic cardiomyopathy and double outlet right ventricle in an infant with down syndrome. |
2013-11-13 |
2023-08-12 |
Not clear |
| Ahmad R Sedaghat, Renee B Flax-Goldenberg, Bob W Gayler, George T Capone, Stacey L Ishma. A case-control comparison of lingual tonsillar size in children with and without Down syndrome. The Laryngoscope. vol 122. issue 5. 2012-07-10. PMID:22374875. |
lingual tonsillar hypertrophy is a common cause of persistent obstructive sleep apnea following adenotonsillectomy in the pediatric population and may be more prevalent in patients with down syndrome (ds). |
2012-07-10 |
2023-08-12 |
Not clear |
| Ioannis M Vlastos, John K Hajiioanno. Clinical practice: diagnosis and treatment of childhood snoring. European journal of pediatrics. vol 169. issue 3. 2010-04-23. PMID:19621244. |
treatment failures or recurrences as well as the existence of causes and contributing factors other than adenotonsillar hypertrophy, like obesity, facial malformations, and down syndrome, have changed the concept of adenotonsillectomy as the ultimate cure. |
2010-04-23 |
2023-08-12 |
Not clear |
| A Wacker, H-G Scheel-Walter, F Neunhoeffe. [Biventricular hypertrophic non-obstructive cardiomyopathy as a symptom of transient myeloproliferative disorder in a newborn with Down syndrome]. Zeitschrift fur Geburtshilfe und Neonatologie. vol 213. issue 2. 2009-06-04. PMID:19319796. |
[biventricular hypertrophic non-obstructive cardiomyopathy as a symptom of transient myeloproliferative disorder in a newborn with down syndrome]. |
2009-06-04 |
2023-08-12 |
Not clear |
| C D Harris, G Ermak, K J A Davie. Multiple roles of the DSCR1 (Adapt78 or RCAN1) gene and its protein product calcipressin 1 (or RCAN1) in disease. Cellular and molecular life sciences : CMLS. vol 62. issue 21. 2006-01-20. PMID:16231093. |
however, chronic expression of the dscr1 (adapt78) gene has now been implicated in several pathological conditions including alzheimer's disease, down syndrome and cardiac hypertrophy. |
2006-01-20 |
2023-08-12 |
human |
| Betty Chan, Garrett Greenan, Frank McKeon, Tom Ellenberge. Identification of a peptide fragment of DSCR1 that competitively inhibits calcineurin activity in vitro and in vivo. Proceedings of the National Academy of Sciences of the United States of America. vol 102. issue 37. 2005-11-09. PMID:16131541. |
one such inhibitor, down syndrome critical region 1 (dscr1), functions in t cell activation, cardiac hypertrophy, and angiogenesis. |
2005-11-09 |
2023-08-12 |
Not clear |
| Thomas Erler, Ekkehart Padit. Obstructive sleep apnea syndrome in children: a state-of-the-art review. Treatments in respiratory medicine. vol 3. issue 2. 2004-07-06. PMID:15182212. |
these include hypertrophy of the tonsils and syndromes such as down syndrome, pickwickian syndrome, prader-willi syndrome or marfan syndrome. |
2004-07-06 |
2023-08-12 |
Not clear |
| Jin Il Lee, Bijaya Kumar Dhakal, Jungsoo Lee, Jaya Bandyopadhyay, Sang Young Jeong, Soo Hyun Eom, Do Han Kim, Joohong Ahn. The Caenorhabditis elegans homologue of Down syndrome critical region 1, RCN-1, inhibits multiple functions of the phosphatase calcineurin. Journal of molecular biology. vol 328. issue 1. 2003-05-13. PMID:12684004. |
a conserved family of calcineurin-regulating proteins whose members have been implicated in several disease models such as down syndrome, alzheimer's disease, and cardiac hypertrophy has been identified in several organisms including yeast, mice, and humans. |
2003-05-13 |
2023-08-12 |
mouse |
| B W Eidem, C Jones, F Cett. Unusual association of hypertrophic cardiomyopathy with complete atrioventricular canal defect and Down syndrome. Texas Heart Institute journal. vol 27. issue 3. 2001-03-08. PMID:11093415. |
unusual association of hypertrophic cardiomyopathy with complete atrioventricular canal defect and down syndrome. |
2001-03-08 |
2023-08-12 |
Not clear |
| S C Kao, L V Muir, K Kimur. Combined hypertrophic pyloric stenosis and duodenal web in Down syndrome: sonographic and radiographic diagnosis. Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine. vol 15. issue 6. 1996-10-17. PMID:8738993. |
combined hypertrophic pyloric stenosis and duodenal web in down syndrome: sonographic and radiographic diagnosis. |
1996-10-17 |
2023-08-12 |
Not clear |
| C M Bower, D Richmon. Tonsillectomy and adenoidectomy in patients with Down syndrome. International journal of pediatric otorhinolaryngology. vol 33. issue 2. 1996-01-16. PMID:7499046. |
tonsillectomy and adenoidectomy in patients with down syndrome usually relieves symptoms of upper airway obstruction due to adenotonsillar hypertrophy. |
1996-01-16 |
2023-08-12 |
Not clear |