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Ankyloblephron Filiform Adnatum: A Case Report.

Divya Jain, Tapas Bandyopadhyay, Vasudha Tomar

Nepalese Journal of Ophthalmology : a Biannual Peer-Reviewed Academic Journal of the Nepal Ophthalmic Society : NEPJOPH

|September 17, 2019

Summary

This summary is machine-generated.

Ankyloblephron filiform adnatum (AFA) is a rare congenital anomaly. Early AFA treatment is crucial to prevent vision loss, and this case highlights a unique association with atrial septal defect.

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Area of Science:

Ophthalmology
Pediatrics
Cardiology

Background:

Ankyloblephron filiform adnatum (AFA) is a rare benign congenital anomaly.
AFA can occur in isolation or as part of a genetic syndrome.
Early intervention for AFA is recommended due to its ambylogenic potential.

Observation:

This report details a newborn diagnosed with sporadic AFA at birth.
The infant presented with an associated Atrial Septal Defect (ASD).

Findings:

The newborn with sporadic AFA and ASD was successfully managed.
This represents the first reported case of sporadic AFA associated with ASD in the medical literature.

Implications:

This case expands the known clinical spectrum of AFA.
Highlights the importance of comprehensive evaluation in newborns with AFA.
Suggests a potential, previously unreported, association between AFA and cardiac anomalies like ASD.