A new variant of MYCN gene as a cause of Feingold syndrome-Reference-Cited by-同舟云学术

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A new variant of MYCN gene as a cause of Feingold syndrome

Published:2022-05 Issue:5 Volume:10 Page:
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clinical Case Reports

Author:

Zeka Naim¹,Bejiqi Ramush²³,Gerguri Abdurrahim¹,Zogaj Leonore¹,Jashari Haki¹⁴^ORCID

Affiliation:

1. Pediatric Clinic Department of Neurology University Clinical Center of Kosovo Pristina Kosovo

2. Pediatric Clinic Department of Cardiology University Clinical Center of Kosovo Pristina Kosovo

3. Faculty of Medicine University of Gjakova Pristina Kosovo

4. Pediatric Clinic University Children’s Hospital Skopje Republic of North Macedonia

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.5886

Reference17 articles.

1. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay

2. Feingold syndrome associated with two novelMYCNmutations in sporadic and familial cases including monozygotic twins

3. Feingold syndrome: Clinical review and genetic mapping

4. Genotype-phenotype correlations in MYCN-related Feingold syndrome

5. Expanding the clinical spectrum ofMYCN-related Feingold syndrome

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