Cystic Fibrosis in a Female Infant with Cardiac, Ocular, and Musculoskeletal Anomalies

Abstract EN

Cystic fibrosis (CF) remains the most common hereditary disease in the western population.

Its concomitant presence with other congenital abnormalities is a rare phenomenon with very little documentation.

In this case report we describe a case of cystic fibrosis in a female infant with cardiac, ocular, and musculoskeletal abnormalities.

A brief literature review is also provided.