Work

Juvenile Hyaline Fibromatosis Syndrome: A Novel Variant in the ANTXR2 Gene Causing Severe Phenotype

Year: 2025

Type: article

Study design: Case Report

Source: Pediatric Dermatology

DOI: 10.1111/pde.70027

Authors: Ilayda Akyon, Ozgenur Ozen, Mustafa Dogan, Zafer Turkoglu, Dilay Bastug, Fatmagul Kusku Cabuk, Alper Gezdirici

Institutions: Sağlık Bilimleri Üniversitesi, İstanbul Başakşehir Çam ve Sakura Şehir Hastanesi

Language: English

Topic: Genetic and rare skin diseases.

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4414030771

FWCI:

Cites: 15

Cited by:

Related to: 10