A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1-Reference-Cited by-同舟云学术

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Published:2020-09-10 Issue:2 Volume:30 Page:71-75
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Peleg Amir,Kurolap Alina,Sagi-Dain Lena,Larom-Khan G.,Adir V.,Mory Adi,Paperna Tamar,Shuldiner A.R.,Gonzaga-Jauregui C.,Adir Noam,Baris Feldman Hagit,Wollstein R.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins.;Blaumeiser;Am J Med Genet A,2008

2. Congenital absence of flexor pollicis longus tendon without associated anomalies of thumb hypoplasia: a case report and review of the literature.;Demirseren;Hand (N Y),2007

3. Evolution and homologies of primate and modern human hand and forearm muscles, with notes on thumb movements and tool use.;Diogo;J Hum Evol,2012

4. Expanding the phenotype of feingold syndrome-2.;Grote;Am J Med Genet A,2015

5. A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4.;Hershkovitz;J Hum Genet,2019

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1. A new variant of MYCN gene as a cause of Feingold syndrome;Clinical Case Reports;2022-05