CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy

c.1918T>G variant identified in this patient further expands the understanding of the genetic spectrum of HJMD in the region.

Authors

Institutions

Publication Details

Journal
Cureus
Published
2026-04-06
DOI
https://doi.org/10.7759/cureus.106554
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy

Enam Danish, Hamza Baeshen, Rola Alsulami
Cureus
Retinal Development and Disorders
article

CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy

Enam Danish, Hamza Baeshen, Rola Alsulami
article en

Abstract

c.1918T>G variant identified in this patient further expands the understanding of the genetic spectrum of HJMD in the region.

CureusVol. 18(4)
University of Jeddah (SA), King Fahd Armed Forces Hospital (SA), King Abdullah Medical City (SA)
Openalex Percentile: Top 32%
Retinal Development and Disorders
DOIOpen Access PDFOpenAlex
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.