Work

Congenital Corneal Staphyloma in an Asian Infant With Kabuki Syndrome Confirmed by a KMT2D Mutation

Year: 2026

Type: article

Study design: Case Report

Source: Journal of Craniofacial Surgery

DOI: 10.1097/scs.0000000000012650

Authors: Hee Jin Yoon, Jung Hyo Ahn

Institutions: Pusan National University Yangsan Hospital, Pusan National University

Language: English

Topic: Ocular Disorders and Treatments

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W7140230249

FWCI:

Cites: 9

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