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Updated: Jun 19, 2026

A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts

A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts

Published on: September 20, 2018

Ascher syndrome: a case report.

Ram Chander¹, Jyoti Mal, Arpita Jain

¹Department of Dermatology and STDs, Lady Hardinge Medical College, New Delhi, India. dr_ram41@yahoo.co.in

Pediatric Dermatology

|October 21, 2009

Summary

This summary is machine-generated.

Ascher syndrome, a rare condition, involves recurrent eyelid swelling. This case highlights a potential forme fruste in an 8-year-old, emphasizing the need for early diagnosis of this rare eye disease.

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Area of Science:

Ophthalmology
Rare Diseases
Pediatric Eye Conditions

Background:

Ascher syndrome is a rare congenital condition, first described in 1920.
It is characterized by recurrent, bilateral upper eyelid swelling and often associated with a double upper lip.
Diagnosis can be challenging due to its rarity and variable presentation.

Observation:

A case report of an 8-year-old child with persistent, recurring swelling of both upper eyelids.
The child's presentation was recalcitrant to standard treatments.
This clinical picture suggested a possible atypical or incomplete form of Ascher syndrome.

Findings:

The patient exhibited symptoms consistent with a forme fruste of Ascher syndrome.
Recalcitrant bilateral upper eyelid edema in a pediatric patient.
This presentation expands the known spectrum of Ascher syndrome manifestations.

Implications:

Early recognition of forme fruste Ascher syndrome is crucial for appropriate management.
This case underscores the importance of considering rare ophthalmological conditions in pediatric patients with recurrent eyelid swelling.
Further research into the genetic and clinical spectrum of Ascher syndrome is warranted.