Leptochoroid in a Case of Alagille Syndrome (Arteriohepatic Dysplasia)

Ophthalmology. 2017 Aug;124(8):1135. doi: 10.1016/j.ophtha.2017.01.024.

Authors

Jen-Hsiang Shen¹, Kuan-Jen Chen², Nan-Kai Wang²

Affiliations

¹ Department of Ophthalmology, Chang Gung Memorial Hospital, Linkou Medical Center, Taoyuan, Taiwan.
² Department of Ophthalmology, Chang Gung Memorial Hospital, Linkou Medical Center, Taoyuan, Taiwan; College of Medicine, Chang Gung University, Taoyuan, Taiwan.

PMID: 28734329
DOI: 10.1016/j.ophtha.2017.01.024

No abstract available

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple / diagnosis
Abnormalities, Multiple / etiology
Alagille Syndrome / complications*
Alagille Syndrome / diagnosis
Alagille Syndrome / genetics
Child
Choroid Diseases / diagnosis
Choroid Diseases / etiology*
Humans
Jagged-1 Protein / genetics
Male
Sequence Analysis, DNA
Slit Lamp Microscopy
Tomography, Optical Coherence

Substances

JAG1 protein, human
Jagged-1 Protein