Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature-Reference-Cited by-同舟云学术

Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature

Published:2021-09-12 Issue:10 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Sassi Hela¹²^ORCID,Elaribi Yasmina¹²,Jilani Houweyda¹²,Rejeb Imen¹,Hizem Syrine¹²,Sebai Molka¹²,Kasdallah Nadia²³,Bouthour Habib²⁴,Hannachi Samia²⁵,Beygo Jasmin⁶^ORCID,Saad Ali⁷⁸,Buiting Karin⁶,H’mida Ben‐Brahim Dorra⁷⁸,BenJemaa Lamia¹²

Affiliation:

1. Department of Congenital and Hereditary Diseases Mongi Slim Hospital Marsa Tunis Tunisia

2. Faculty of Medicine of Tunis University Tunis El Manar Tunis Tunisia

3. Paediatric Department Military Hospital of Tunis Tunis Tunisia

4. Department of Paediatric Surgery Tunis Tunisia

5. Laboratory of Pathology Anatomy and Cytology Tunis Tunisia

6. Institute for Human Genetics Essen University Hospital Essen Germany

7. Department of Cytogenetics and Reproductive Biology Farhat Hached University Hospital Sousse Tunisia

8. Faculty of Medicine of Sousse University of Sousse Sousse Tunisia

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1796

Reference51 articles.

1. Simultaneous occurrence of right adrenocortical tumor and left adrenal neuroblastoma in an infant with Beckwith-Wiedemann syndrome

2. Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe

3. Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of kidneys and pancreas, and leydig‐cell hyperplasia: Another syndrome;Beckwith J. B.;West Society for Pediatric Research,1963

4. Epigenotype and phenotype correlations in patients with beckwith-wiedemann syndrome

5. Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS)

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