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Neuro-rehabilitation Approach for Sudden Sensorineural Hearing Loss
Published on: January 25, 2016
Keratitis-ichthyosis-deafness (KID) syndrome.
Mercedes E Gonzalez1, Brook E Tlougan, Harper N Price
1Department of Dermatology, New York University, USA.
Dermatology Online Journal
|November 7, 2009
Summary
Keratitis-ichthyosis-deafness (KID) syndrome presents with skin, hearing, and eye issues. This case highlights scalp infections and cysts as potential KID syndrome manifestations, emphasizing cancer risks.
Area of Science:
- Dermatology
- Genetics
- Otolaryngology
Background:
- Keratitis-ichthyosis-deafness (KID) syndrome is a rare genetic disorder.
- It is characterized by a triad of ocular, cutaneous, and auditory abnormalities.
Observation:
- A 21-year-old male presented with congenital skin anomalies including diffuse skin thickening, verrucous plaques, and palmoplantar keratoderma.
- The patient also exhibited sensorineural hearing loss and keratoconjunctivitis, consistent with KID syndrome.
- He reported a history of recurrent scalp infections, cysts, and inflammatory nodules.
Findings:
- This case underscores scalp manifestations such as folliculitis, cysts, and recurrent infections as potential features of KID syndrome.
- The study highlights the association between KID syndrome and an increased risk of follicular tumors and squamous-cell carcinomas.
Implications:
- Early recognition of diverse KID syndrome presentations, including scalp issues, is crucial for timely management.
- Increased awareness of oncological risks in KID syndrome patients is warranted for proactive surveillance and treatment.
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