Case report describes craniofacial and dental anomalies in a 2-year-old male, highlighting the need for early diagnosis and interdisciplinary management.
Key Points
To present a rare case of Hallermann–Streiff syndrome in a young child and emphasize the importance of early diagnosis and treatment.
Case report of a 2-year-old male with clinical signs and radiological findings indicative of HSS.
Multidisciplinary management involving specialists for functional treatment of ocular, dental, skeletal, and respiratory conditions.
Distinct craniofacial and dental anomalies were observed in the patient.
Early diagnosis and interdisciplinary treatment significantly improved the patient's functional outcomes.