Feingold Syndrome Latest Advances

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 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

Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report.

Journal: Frontiers in pediatrics

Published: September 26, 2021

Genome sequencing identifies three molecular diagnoses including a mosaic variant in the COL2A1 gene in an individual with Pol III-related leukodystrophy and Feingold syndrome.

Journal: Cold Spring Harbor molecular case studies

Published: August 11, 2021

Filters

Feingold syndrome with GJB2 variants.

Feingold syndrome with GJB2 variants.

Rare features in Feingold syndrome type 1.

Rare features in Feingold syndrome type 1.

MYCN in human development and diseases.

MYCN in human development and diseases.

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

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

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

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

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

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

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

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

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

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

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

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

Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report.

Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report.

Genome sequencing identifies three molecular diagnoses including a mosaic variant in the COL2A1 gene in an individual with Pol III-related leukodystrophy and Feingold syndrome.

Genome sequencing identifies three molecular diagnoses including a mosaic variant in the COL2A1 gene in an individual with Pol III-related leukodystrophy and Feingold syndrome.