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Quoted phrase not found in phrase index: "Lymphedema-atrial septal defects-facial changes syndrome"
Page 1
National population-based estimates for major birth defects, 2010-2014.
Mai CT, Isenburg JL, Canfield MA, Meyer RE, Correa A, Alverson CJ, Lupo PJ, Riehle-Colarusso T, Cho SJ, Aggarwal D, Kirby RS; National Birth Defects Prevention Network. Mai CT, et al. Birth Defects Res. 2019 Nov 1;111(18):1420-1435. doi: 10.1002/bdr2.1589. Epub 2019 Oct 3. Birth Defects Res. 2019. PMID: 31580536 Free PMC article.
While the birth prevalence of most birth defects studied remained relatively stable over 15 years, an increasing prevalence was observed for gastroschisis and Down syndrome. Additionally, the prevalence for atrioventricular septal defect, tetralogy of Fallot, …
While the birth prevalence of most birth defects studied remained relatively stable over 15 years, an increasing prevalence was observed …
Holt-Oram syndrome.
Smith AT, Sack GH Jr, Taylor GJ. Smith AT, et al. J Pediatr. 1979 Oct;95(4):538-43. doi: 10.1016/s0022-3476(79)80758-1. J Pediatr. 1979. PMID: 480027
The autosomal dominant association of upper extremity skeletal defects with congenital heart disease is known as the Holt-Oram syndrome. We reviewed our experience with 39 affected patients of whom 15 were considered new mutations. Wide varieties of skeletal defects and co …
The autosomal dominant association of upper extremity skeletal defects with congenital heart disease is known as the Holt-Oram syndrome …
SARS: radiological features.
Ooi GC, Daqing M. Ooi GC, et al. Respirology. 2003 Nov;8 Suppl(Suppl 1):S15-9. doi: 10.1046/j.1440-1843.2003.00519.x. Respirology. 2003. PMID: 15018128 Free PMC article. Review.
Generally, radiographic opacities peak between 8 and 10 days after onset of illness, with radiographic scores reflecting temporal changes in clinical and laboratory parameters such as oxygen saturation (SaO2) and liver transaminases. ...Temporal lung changes …
Generally, radiographic opacities peak between 8 and 10 days after onset of illness, with radiographic scores reflecting temporal …
Clinical and genetic findings in patients with congenital cataract and heart diseases.
Li X, Si N, Song Z, Ren Y, Xiao W. Li X, et al. Orphanet J Rare Dis. 2021 May 31;16(1):242. doi: 10.1186/s13023-021-01873-7. Orphanet J Rare Dis. 2021. PMID: 34059112 Free PMC article.
In clinical practice, the concurrence of CC and CHD is frequently observed in patients. Additionally, some monogenic diseases, copy number variation (CNV) syndromes, and diseases associated with intrauterine infection involve both cataract and heart defects. ...The …
In clinical practice, the concurrence of CC and CHD is frequently observed in patients. Additionally, some monogenic diseases, copy n …
Williams-Beuren syndrome: computed tomography imaging review.
Das KM, Momenah TS, Larsson SG, Jadoon S, Aldosary AS, Lee EY. Das KM, et al. Pediatr Cardiol. 2014 Dec;35(8):1309-20. doi: 10.1007/s00246-014-0998-z. Epub 2014 Aug 20. Pediatr Cardiol. 2014. PMID: 25139247 Review.
Williams-Beuren syndrome (WBS) affects young infants and children. The underlying etiopathogenesis of this rare disease is due to the mutation of the elastin gene that is responsible for the elasticity of the arterial wall. ...The most common cardiovascular abnormalities e …
Williams-Beuren syndrome (WBS) affects young infants and children. The underlying etiopathogenesis of this rare disease is due to the …
Acute Cardiac Effects of Severe Pre-Eclampsia.
Vaught AJ, Kovell LC, Szymanski LM, Mayer SA, Seifert SM, Vaidya D, Murphy JD, Argani C, O'Kelly A, York S, Ouyang P, Mukherjee M, Zakaria S. Vaught AJ, et al. J Am Coll Cardiol. 2018 Jul 3;72(1):1-11. doi: 10.1016/j.jacc.2018.04.048. J Am Coll Cardiol. 2018. PMID: 29957219 Free PMC article.

METHODS: In this prospective observational study, the authors recruited 63 women with PEC and 36 pregnant control patients. ...For left-sided cardiac parameters, there were differences (p < 0.001) in mitral septal e' velocity (9.6 2.4 cm/s vs. 11.6 1.9 cm/s),

…
METHODS: In this prospective observational study, the authors recruited 63 women with PEC and 36 pregnant control patients. ...For le …
The Impact of Technology on the Diagnosis of Congenital Malformations.
Straub L, Huybrechts KF, Bateman BT, Mogun H, Gray KJ, Holmes LB, Hernandez-Diaz S. Straub L, et al. Am J Epidemiol. 2019 Nov 1;188(11):1892-1901. doi: 10.1093/aje/kwz153. Am J Epidemiol. 2019. PMID: 31241162 Free PMC article.
Trends were not explained by changes in the prevalence of risk factors but were attenuated when accounting for screening tests. ...Findings suggest that increased screening partially explains the observed increase in diagnosis of milder cases of select common malfor …
Trends were not explained by changes in the prevalence of risk factors but were attenuated when accounting for screening tests. ...Fi …
National population-based estimates for major birth defects, 2016-2020.
Stallings EB, Isenburg JL, Rutkowski RE, Kirby RS, Nembhard WN, Sandidge T, Villavicencio S, Nguyen HH, McMahon DM, Nestoridi E, Pabst LJ; National Birth Defects Prevention Network. Stallings EB, et al. Birth Defects Res. 2024 Jan;116(1):e2301. doi: 10.1002/bdr2.2301. Birth Defects Res. 2024. PMID: 38277408 Free PMC article.
RESULTS: Adjusted national prevalence estimates per 10,000 live births ranged from 0.63 for common truncus to 18.65 for clubfoot. Temporal changes were observed for several birth defects, including increases in the prevalence of atrioventricular septal defect …
RESULTS: Adjusted national prevalence estimates per 10,000 live births ranged from 0.63 for common truncus to 18.65 for clubfoot. Temporal …
Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature.
Homma TK, Freire BL, Honjo R, Dauber A, Funari MFA, Lerario AM, Albuquerque EVA, Vasques GA, Bertola DR, Kim CA, Malaquias AC, Jorge AAL. Homma TK, et al. Horm Res Paediatr. 2019;92(2):115-123. doi: 10.1159/000503782. Epub 2019 Nov 12. Horm Res Paediatr. 2019. PMID: 31715605 Review.
BACKGROUND: Floating-Harbor syndrome (FHS) is a rare condition characterized by dysmorphic facial features, short stature, and expressive language delay. ...The median height changes during the treatment period (approx. 2.9 years) were 1.1 SDS (range from -0.4 to 3. …
BACKGROUND: Floating-Harbor syndrome (FHS) is a rare condition characterized by dysmorphic facial features, short stature, and expres …
Subcutaneous Sweet syndrome in the setting of myeloid disorders: a case series and review of the literature.
Chan MP, Duncan LM, Nazarian RM. Chan MP, et al. J Am Acad Dermatol. 2013 Jun;68(6):1006-15. doi: 10.1016/j.jaad.2012.12.954. Epub 2013 Feb 8. J Am Acad Dermatol. 2013. PMID: 23399459 Review.
No myeloid blasts, vascular changes, or non-Miescher granulomas were observed. No micro-organisms were identified in the skin nodules. ...CONCLUSIONS: Based on the fairly consistent clinical and histologic findings, neutrophilic panniculitis occurring in the setting …
No myeloid blasts, vascular changes, or non-Miescher granulomas were observed. No micro-organisms were identified in the skin …
132 results