Rhinologic Manifestations of Ectodermal Dysplasia

Author:

Mehta Umang1,Brunworth Joseph1,Lewis Richard Alan2,Sindwani Raj1

Affiliation:

1. Department of Otolaryngology–Head and Neck Surgery, St. Louis University, St. Louis, Missouri

2. Departments of Ophthalmology, Medicine, Pediatrics, and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas

Abstract

Background The Ectodermal Dysplasias (ED) are a group of uncommon genetic disorders characterized by deficient development of tissues derived from ectoderm and mesoderm. Abnormalities of the respiratory epithelium prevent normal mucociliary function. We explored the prevalence and severity of sinonasal features in affected individuals. Methods Thirty-four subjects with ED were evaluated. A focused history and thorough nasal examination including flexible nasopharyngoscopy were performed. Patients and caregivers rated the severity of rhinologic symptoms with a standard scale. Standardized smell tests were also performed. Results The study included 21 males and 13 females whose mean age was 18.8 years (range, 4 months to 85 years). The majority (79%) had Hypohydrotic ED. Nearly half of the individuals evaluated reported moderate to severe nasal obstruction. Allergic symptoms were present in 44% of individuals whereas 41% had a history of sinusitis. Nasal concretions were significantly more troublesome in those aged 15 and under (p = 0.028). Eighteen percent had undergone sinonasal surgery. On examination, normal intranasal structures were identifiable in all patients. However, dry mucosae, prominent crusts, and concretions were found in most (79%). A deviated nasal septum was present in 23% of individuals and a saddle nose deformity in 18. Smell tests were normal for age in all subjects. Conclusion Rhinologic issues are prevalent and problematic in individuals with ED. Management should focus on humidification, nasal debridement, and tailored therapy for allergic rhinitis and sinusitis. Increased awareness of the sinonasal concerns in ED will facilitate diagnosis and improve the care of these patients.

Publisher

SAGE Publications

Subject

Otorhinolaryngology

Reference14 articles.

1. Freire-MaiaN., and PinheiroM. Ectodermal Dysplasias: A Clinical and Genetic Study, Vol. 26. New York: Alan R. Liss, 72–74, 1984.

2. HEREDITARY ECTODERMAL DYSPLASIA (CONGENITAL ECTODERMAL DEFECT)

3. Ectodermal Dysplasia: Otolaryngologic Manifestations and Management

4. Towards a new classification of ectodermal dysplasias

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