مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

Cornelia de Lange Syndrome: A Case Report with a Novel Congenital Heart Disease Association

Pages

  00-00

Abstract

 Introduction: Cornelia de Lange Syndrome (CdLS) is a rare non-hereditary syndrome. The key diagnosis is unique facial features, limb anomalies, and growth retardation. Cardiac defects with gastrointestinal and genitourinary anomalies may be associated. Case Presentation: This is a case of neonatal CdLS that we think is interesting due to its association with a novel congenital heart complex. Conclusions: Patients with CdLS have a high incidence of congenital heart disease (CHD), so a cardiologic study of all of these patients is suggested.

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  • Cite

    APA: Copy

    D. Allugmani, Mohammad, K. El Harbi, Mazen, Khoshhal, Mohammad S., Alrabghy, Najia, Almutery, Sabreen, D. Alawfi, Abdulsalam, & M. Abo Haded, Hany. (2022). Cornelia de Lange Syndrome: A Case Report with a Novel Congenital Heart Disease Association. JOURNAL OF COMPREHENSIVE PEDIATRICS, 13(4), 00-00. SID. https://sid.ir/paper/1118253/en

    Vancouver: Copy

    D. Allugmani Mohammad, K. El Harbi Mazen, Khoshhal Mohammad S., Alrabghy Najia, Almutery Sabreen, D. Alawfi Abdulsalam, M. Abo Haded Hany. Cornelia de Lange Syndrome: A Case Report with a Novel Congenital Heart Disease Association. JOURNAL OF COMPREHENSIVE PEDIATRICS[Internet]. 2022;13(4):00-00. Available from: https://sid.ir/paper/1118253/en

    IEEE: Copy

    Mohammad D. Allugmani, Mazen K. El Harbi, Mohammad S. Khoshhal, Najia Alrabghy, Sabreen Almutery, Abdulsalam D. Alawfi, and Hany M. Abo Haded, “Cornelia de Lange Syndrome: A Case Report with a Novel Congenital Heart Disease Association,” JOURNAL OF COMPREHENSIVE PEDIATRICS, vol. 13, no. 4, pp. 00–00, 2022, [Online]. Available: https://sid.ir/paper/1118253/en

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