Feingold Syndrome Latest Advances

Turner's Syndrome in Discordant Dizygotic Twins: Biological Origins and Twin Relations/Twin Research Reviews: Prevention of Premature Twin Birth; Twin Gestation with Hydatidiform Mole; Update on Feingold Syndrome Twins; Qualitative MZ Twin Difference Studies/Media: Identical Twins Turn 100 Years of Age; Twins in Famous Families; Celebration of Yorùbá Twins of Nigeria; Identical Artistic Partners; Rare Conjoined Twins Separated.

Journal: Twin research and human genetics : the official journal of the International Society for Twin Studies

Published: December 04, 2025

Twins in Naturalistic Context: Highlights from the International Society for Human Ethology/Twin Research Reviews: Twins with Feingold Syndrome; Twins' Language Delays; Breastfeeding Twins; Twins with Olmsted Syndrome/In the News: Loss of Texas Twins; A Singular Musical Sensation; Conjoined Twin Deliveries in Myanmar and India; Major League Baseball Pairs.

Journal: Twin research and human genetics : the official journal of the International Society for Twin Studies

Published: September 09, 2025

Feingold syndrome with GJB2 variants.

Journal: Auris, nasus, larynx

Published: May 14, 2025

Rare features in Feingold syndrome type 1.

Journal: European journal of medical genetics

Published: November 19, 2024

Mycn regulates vascular development through PI3K signaling pathway in zebrafish.

Journal: Developmental dynamics : an official publication of the American Association of Anatomists

Published: September 14, 2024

MYCN in human development and diseases.

Journal: Frontiers in oncology

Published: April 15, 2024

Gain-of-function MYCN causes a megalencephaly-polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome.

Journal: HGG advances

Published: June 16, 2023

Feingold syndrome type 1: a rare cause of fetal microcephaly (prenatal diagnosis).

Journal: BMJ case reports

Published: March 08, 2023

Mycn regulates intestinal development through ribosomal biogenesis in a zebrafish model of Feingold syndrome 1.

Journal: PLoS biology

Published: May 03, 2022

Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia.

Journal: American journal of medical genetics. Part A

Published: March 01, 2022

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

Journal: Clinical case reports

Published: February 20, 2022

First Patient Diagnosed as Feingold Syndrome Type 2 with Alport Syndrome and Review of the Current Literature.

Journal: Molecular syndromology

Published: November 24, 2021