Feeding Difficulty in an Infant with Stickler's Syndrome
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Updated: Dec 23, 2025

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Published on: February 5, 2019
Parvathy Vijay1, Parvathy Kumaran1, Arun Mamachan Xavier1
1Department of Pedodontics and Preventive Dentistry, Amrita School of Dentistry, Amrita Institute of Medical Sciences, Amrita University, Kochi, Kerala, India.
Insights
Stickler syndrome, a genetic disorder, can cause severe feeding issues in infants. This case report highlights the clinical presentation, diagnosis, and management of a 48-day-old infant with this condition.
Area of Science:
- Genetics
- Ophthalmology
- Pediatrics
Background:
- Stickler syndrome is an autosomal dominant disorder affecting connective tissues.
- It presents with variable ocular, skeletal, orofacial, and auditory symptoms.
Observation:
- A 48-day-old infant experienced severe feeding difficulties.
- Clinical examination revealed features consistent with Stickler syndrome.
Findings:
- The case report details the diagnostic process for Stickler syndrome in an infant.
- It emphasizes the importance of early identification of feeding difficulties.
Implications:
- Early diagnosis and management of Stickler syndrome are crucial for infant development.
- This case contributes to understanding the pediatric manifestations of Stickler syndrome.
Abstract:
Stickler syndrome or hereditary progressive arthro-ophthalmopathy is an autosomal dominant condition characterized by ocular manifestations, arthritic changes, orofacial features, and deafness, in variable degrees. This is a case report of a 48-day-old infant who presented with severe feeding difficulty. It also details the clinical, diagnostic features, and management of an infant with Stickler syndrome.
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