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Quoted phrase not found in phrase index: "Congenital heart defects, multiple types, 6"
Page 1
VACTERL/VATER Association.
Solomon BD. Solomon BD. Orphanet J Rare Dis. 2011 Aug 16;6:56. doi: 10.1186/1750-1172-6-56. Orphanet J Rare Dis. 2011. PMID: 21846383 Free PMC article. Review.
VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. ...The managemen …
VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral …
Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type compared to other heritable connective tissue disorders.
Colombi M, Dordoni C, Chiarelli N, Ritelli M. Colombi M, et al. Am J Med Genet C Semin Med Genet. 2015 Mar;169C(1):6-22. doi: 10.1002/ajmg.c.31429. Am J Med Genet C Semin Med Genet. 2015. PMID: 25821090 Review.
In this review, we revise the differential diagnosis of JHS/EDS-HT with those heritable connective tissue disorders which show a significant overlap with the former and mostly include EDS classic, vascular and kyphoscoliotic types, osteogenesis imperfecta, Marfan syndrome, …
In this review, we revise the differential diagnosis of JHS/EDS-HT with those heritable connective tissue disorders which show a significant …
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.
The clinical features of the congenital heart defects in the patients with KS were summarized. RESULTS: Congenital heart defects were one of the clinical manifestations of KS with 90.6% of the patients being diagnosed prenatally or …
The clinical features of the congenital heart defects in the patients with KS were summarized. RESULTS: Congenital
Co-occurring anomalies in congenital oral clefts.
Stoll C, Alembik Y, Roth MP. Stoll C, et al. Am J Med Genet A. 2022 Jun;188(6):1700-1715. doi: 10.1002/ajmg.a.62689. Epub 2022 Feb 18. Am J Med Genet A. 2022. PMID: 35179301
Oral clefts (OCs) are frequently co-occurring with other non-OC congenital anomalies. The types and the prevalence of anomalies co-occurring with OCs vary in the reported studies. ...The most frequent MCA were in the musculoskeletal system (16.7%), the central nervo …
Oral clefts (OCs) are frequently co-occurring with other non-OC congenital anomalies. The types and the prevalence of anomalie …
Partial Anomalous Left Pulmonary Artery Anterior Versus Posterior Types: A Systematic Review.
Restrepo CS, Gonzalez TV, Baxi AJ, Saboo SS. Restrepo CS, et al. Tomography. 2022 Jul 27;8(4):1947-1958. doi: 10.3390/tomography8040163. Tomography. 2022. PMID: 36006061 Free PMC article. Review.
PALPAs were more commonly anterior than posterior. Mean age: 5.3 years (SD = 12.4) for anterior and 6.8 years (SD = 18.5) for posterior (p = 0.77). Respiratory symptoms: 20% of anterior and 60% of posterior cases (p = 0.032). ...Non-cardiac and non-tracheobronchial anomali …
PALPAs were more commonly anterior than posterior. Mean age: 5.3 years (SD = 12.4) for anterior and 6.8 years (SD = 18.5) for posteri …
Perinatal outcomes and congenital heart defect prognosis in 53313 non-selected perinatal infants.
Xie D, Wang H, Liu Z, Fang J, Yang T, Zhou S, Wang A, Qin J, Xiong L. Xie D, et al. PLoS One. 2017 Jun 7;12(6):e0177229. doi: 10.1371/journal.pone.0177229. eCollection 2017. PLoS One. 2017. PMID: 28591192 Free PMC article.
OBJECTIVE: To evaluate perinatal outcomes and congenital heart defect (CHD) prognosis in a non-selected population. ...RESULTS: In total, 190 CHD cases were identified among the 53313 included perinatal infants (PIs), indicating a CHD prevalence of 35.64 per 10000 P …
OBJECTIVE: To evaluate perinatal outcomes and congenital heart defect (CHD) prognosis in a non-selected population. ...RESULTS …
Procedural Risk in Congenital Cardiac Catheterization (PREDIC(3)T).
Quinn BP, Yeh M, Gauvreau K, Ali F, Balzer D, Barry O, Batlivala S, Berman D, Foerster S, Goldstein B, Hainstock M, Holzer R, Janssen D, O'Byrne ML, Shirley L, Trucco S, Whiteside W, Bergersen L. Quinn BP, et al. J Am Heart Assoc. 2022 Jan 4;11(1):e022832. doi: 10.1161/JAHA.121.022832. Epub 2021 Dec 22. J Am Heart Assoc. 2022. PMID: 34935425 Free PMC article.
Background Advancements in the field, including novel procedures and multiple interventions, require an updated approach to accurately assess patient risk. ...Thirty-four unique case types were determined and stratified into 6 risk categories. Six hemodynamic …
Background Advancements in the field, including novel procedures and multiple interventions, require an updated approach to accuratel …
Strengths, Limitations, and Geographical Discrepancies in the Eligibility Criteria for Sport Participation in Young Patients With Congenital Heart Disease.
Cantinotti M, Giordano R, Assanta N, Murzi B, Melo M, Franchi E, Crocetti M, Iervasi G, Kutty S. Cantinotti M, et al. Clin J Sport Med. 2018 Nov;28(6):540-560. doi: 10.1097/JSM.0000000000000474. Clin J Sport Med. 2018. PMID: 28742603 Review.
Eligibility criteria were consistent between countries for simple congenital heart defects, whereas there are discrepancies for borderline conditions including moderate valvular lesions and mild or moderate residual defects after CHD repair. Furthermor …
Eligibility criteria were consistent between countries for simple congenital heart defects, whereas there are discrepan …
Neuroradiographic findings in 22q11.2 deletion syndrome.
Bohm LA, Zhou TC, Mingo TJ, Dugan SL, Patterson RJ, Sidman JD, Roby BB. Bohm LA, et al. Am J Med Genet A. 2017 Aug;173(8):2158-2165. doi: 10.1002/ajmg.a.38304. Epub 2017 Jun 3. Am J Med Genet A. 2017. PMID: 28577347 Free article.
The most common indications for imaging were unexplained developmental delay (6/24), seizures of unknown etiology (5/24), and unilateral weakness (3/24). ...These findings reveal the types and frequencies of brain malformations in this case series, and suggest that …
The most common indications for imaging were unexplained developmental delay (6/24), seizures of unknown etiology (5/24), and unilate …
Clinical and epidemiological features of heart-hand syndrome, an updated analysis in China.
Yin Y, Ji J, Zhao J, Chen S, Tian W. Yin Y, et al. BMC Musculoskelet Disord. 2020 Nov 25;21(1):777. doi: 10.1186/s12891-020-03813-1. BMC Musculoskelet Disord. 2020. PMID: 33238988 Free PMC article.
HHS patients had a higher comorbidity rate (11%) than non-HHS patients (6.9%). Patients with HHS were classified into four groups by the types of congenital upper extremity malformations, among which the most common group was thumb type (121/200, 60.5%). CONC …
HHS patients had a higher comorbidity rate (11%) than non-HHS patients (6.9%). Patients with HHS were classified into four groups by …
54 results