Axenfeld-Rieger syndrome: A systematic review examining genetic, neurological, and neurovascular associations to inform screening

Logan Muzyka,Emily Winterhalter,Melissa A. LoPresti, Jonathan Scoville,Brenda L. Bohnsack,Sandi K. Lam

Heliyon（2023）

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摘要

Axenfeld-Rieger Syndrome (ARS) is comprised of a group of autosomal dominant disorders that are each characterized by anterior segment abnormalities of the eye. Mutations in the transcription factors FOXC1 or PITX2 are the most well-studied genetic manifestations of this syndrome.

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syndrome,neurovascular associations,genetic,axenfeld-rieger

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