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Updated: Jan 7, 2026

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Ampliando el espectro fenotípico del síndrome de Axenfeld-Rieger tipo 3 relacionado con FOXC1: un informe de caso

Amia Mourad¹, Harry Ward¹, Nicholas Lorenz²

¹Medicine, Lake Erie College of Osteopathic Medicine, Jacksonville, USA.

|January 5, 2026

Resumen

No abstract available in PubMed .

Palabras clave:

Disgenesis del segmento anterior Síndrome de Axenfeld-Rieger el coloboma Enfermedad cardíaca congénita (CHD)Córrectopia Dismorfismo craneofacial La eliminación de foxc1 Embriotoxinas en la parte posterior Malformación de la fosa posterior pérdida auditiva neurosensorial (sn)

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