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Cardiac anomalies in children with congenital duodenal obstruction: a systematic review with meta-analysis.
Pijpers AGH, Eeftinck Schattenkerk LD, de Vries R, Broers CJM, Straver B, van Heurn ELW, Musters GD, Gorter RR, Derikx JPM. Pijpers AGH, et al. Pediatr Surg Int. 2023 Mar 26;39(1):160. doi: 10.1007/s00383-023-05449-3. Pediatr Surg Int. 2023. PMID: 36967411 Free PMC article. Review.
The most prevalent type of obstruction was type 3 (complete atresias), with a pooled percentage of 54% (95% CI 0.48-0.60). The pooled percentage of Trisomy 21 in patients with DO was 28% (95% CI 0.26-0.31). CONCLUSION: This review shows cardiac anomalies are found i …
The most prevalent type of obstruction was type 3 (complete atresias), with a pooled percentage of 54% (95% CI 0.48-0.60). The pooled …
Prolonged survival in Edwards syndrome with congenital heart disease: a case report and literature review.
López-Ríos V, Grajales-Marín E, Gómez-Zambrano V, Barrios-Arroyave FA. López-Ríos V, et al. Medwave. 2020 Sep 3;20(8):e8015. doi: 10.5867/medwave.2020.08.8015. Medwave. 2020. PMID: 32956340 Review. English, Spanish.
Edwards syndrome or trisomy 18 is a complex entity that involves the musculoskeletal, craniofacial, cardiovascular, and neurological systems. Its genetics are varied, presenting both in a complete and mosaic type. Survival rarely exceeds the first year of lif …
Edwards syndrome or trisomy 18 is a complex entity that involves the musculoskeletal, craniofacial, cardiovascular, and neurol …
[XY type gonadal dysgenesis, trisomy X and variants].
Kikuchi I, Takeuchi H, Kinoshita K. Kikuchi I, et al. Nihon Rinsho. 2004 Feb;62(2):309-12. Nihon Rinsho. 2004. PMID: 14968537 Review. Japanese.
XY gonadal dysgenesis, this is a condition that has XY chromosome but is characterized by the indifferent testis. There are complete and incomplete types. Complete type has bilateral gonads of cordee, does not show physical characteristics of Turner's syndrome …
XY gonadal dysgenesis, this is a condition that has XY chromosome but is characterized by the indifferent testis. There are complete …
Bone marrow transplantation for Behçet's disease: a case report and systematic review of the literature.
Soysal T, Salihoğlu A, Esatoğlu SN, Gültürk E, Eşkazan AE, Hatemi G, Hatemi I, Öngören Aydın Ş, Erzin YZ, Başlar Z, Tüzüner N, Ferhanoğlu B, Çelik AF. Soysal T, et al. Rheumatology (Oxford). 2014 Jun;53(6):1136-41. doi: 10.1093/rheumatology/ket479. Epub 2014 Feb 6. Rheumatology (Oxford). 2014. PMID: 24505123 Review.
RESULTS: A 30-year-old woman with refractory GI BD involvement with trisomy 8 MDS underwent a successful myeloablative allogeneic HSCT resulting in complete resolution of both BD and MDS. ...All of these patients achieved complete remission of GI findings aft …
RESULTS: A 30-year-old woman with refractory GI BD involvement with trisomy 8 MDS underwent a successful myeloablative allogeneic HSC …