Clinical Findings in an Asian Family with Axenfeld-Rieger Syndrome

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A Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings

PURPOSE To describe clinical findings in a Korean family with Axenfeld-Rieger syndrome. METHODS A retrospective review of clinical data about patients with diagnosed Axenfeld-Rieger syndrome. Five affected members of the family underwent a complete ophthalmologic examination. We screened the forkhead box C1 gene and the pituitary homeobox 2 gene in patients. Peripheral blood leukocytes and bu...

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Novel Genetic Findings in a Chinese Family with Axenfeld-Rieger Syndrome

PURPOSE To describe a Chinese family with Axenfeld-Rieger syndrome (ARS) and report our novel genetic findings. METHODS Nine members of the same family underwent complete ophthalmologic examinations and genetic analysis. Genomic DNA was isolated from veinal blood and amplifed using PCR; the products of PCR were sequenced and compared with FOXC1 and PITX2 genes, from which the mutations were f...

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Magnetic resonance imaging findings in Axenfeld–Rieger syndrome

Axenfeld-Rieger syndrome (ARS) is a genetic disorder representing a disease spectrum resulting from neural crest cell maldevelopment. Glaucoma is a common complication from the incomplete formation of the iridocorneal angle structures. Neural crest cells also form structures of the forebrain and pituitary gland, dental papillae, aortic arch walls, genitalia, and long bones; therefore, patients ...

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The Axenfeld syndrome and the Rieger syndrome.

A family is reported in which both the syndrome of Axenfeld and the eye malformations of the syndrome of Rieger occur, indicating that both may be expressions of the same gene. We also review the associated anomalies already reported, emphasise their high incidence, suggest that these are not accidental associations, and propose some possible explanations for the high incidence.

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ژورنال

عنوان ژورنال: Pakistan Journal of Ophthalmology

سال: 2020

ISSN: 0886-3067

DOI: 10.36351/pjo.v36i2.974