Search
ChatPaper
AI Writing
analysis
Analysis
编组
Open Data
more
More
RankingsMust ReadingJournal&ConferenceAI TRAI HistoryMaster Reading TreeXiaomai's Star TalentsTrajectoryTalentNDI TrackerOpenAI sign Language
VIPCreated with Sketch.

Congenital Corneal Opacity in 22q11.2 Deletion Syndrome: A Case Series.

Elena Franco,Naeem Iqbal,Parth R Shah,Michelle Alabek,Kelly S Tripi,Christina Prescott,Hannah L Scanga,Charleen T Chu,Ken K Nischal

Cornea（2023）

Cited 0|Views22
No score
Abstract
22q11.2 DS can rarely be associated with CCO. We describe a consistent pattern of central clearing related to posterior stromal thinning, with or without ICA/KLA. Possible candidate genes for corneal opacification in 22q11.2 DS remain elusive.
More
Translated text
Key words
22q11,2 deletion syndrome,congenital corneal opacity,anterior segment imaging
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined