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Updated: Jun 7, 2026
09:09
Cryosectioning and Immunostaining Mouse Inner Ear Tissue: From Embryonic to Adult Stages
Published on: April 11, 2025
[Hunter's syndrome and hearing impairment]
Eva Kirkegaard Kiaer1, Troels Reinholdt Møller, Randi Wetke
1Otologisk Afdeling, Vejle Sygehus, 7100 Vejle, Denmark. evakirkegaard@hotmail.com
Ugeskrift for Laeger
|November 9, 2010
Summary
A young boy with recurrent ear infections and developmental delays was diagnosed with Hunter Syndrome (Mucopolysaccharidosis type II). Early diagnosis and treatment are crucial for managing this rare genetic disorder.
Area of Science:
- Pediatrics
- Genetics
- Audiology
Background:
- Delayed language development in a 30-month-old boy.
- History of 19 acute otitis media episodes and four tympanostomy tube placements.
Observation:
- Significant delays in motor function and language acquisition.
- Audible respiratory sounds and nasal congestion noted.
- Referred for further pediatric investigations.
Findings:
- Diagnosis of Hunter Syndrome (Mucopolysaccharidosis type II - MPSII).
- Identification of a rare genetic disorder impacting development.
Implications:
- Highlights the importance of comprehensive evaluation for developmental delays.
- Underscores the need for timely diagnosis of rare genetic conditions like MPSII.
- Emphasizes the role of audiology and pediatrics in identifying and managing complex cases.
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