Congenital cataract with global developmental delay and microcephaly in three Tunisian families: A new recessive syndrome?

Congenital cataract is one of the most genetically heterogeneous ocular malformations causing visual impairment and blindness in children.

Authors

Publication Details

Journal
Open Journal of Clinical and Medical Case Reports
Published
2024-10-31
DOI
https://doi.org/10.52768/2379-1039/2299
Primary Topic
Connexins and lens biology
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Congenital cataract with global developmental delay and microcephaly in three Tunisian families: A new recessive syndrome?

Manèl Chograni
Open Journal of Clinical and Medical Case Reports
Connexins and lens biology
article

Congenital cataract with global developmental delay and microcephaly in three Tunisian families: A new recessive syndrome?

Manèl Chograni
article en

Abstract

Congenital cataract is one of the most genetically heterogeneous ocular malformations causing visual impairment and blindness in children.

Open Journal of Clinical and Medical Case ReportsVol. 10(24)
Openalex Percentile: Top 77%
Connexins and lens biology
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.

Congenital cataract with global developmental delay and microcephaly in three Tunisian families: A new recessive syndrome? — Manèl Chograni · Open Journal of Clinical and Medical Case Reports (2024) | TGRS Research Map | TGRS