Short Cilia, Immunodeficiency, and Cystic Fibrosis in a Mother-Daughter Pair

0Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Patients with chronic rhinosinusitis (CRS) that is refractory to maximal medical and surgical therapy should be evaluated for other primary conditions. Cystic fibrosis (CF), primary immunodeficiency (PID), and primary ciliary dyskinesia (PCD) are potential risk factors for refractory CRS. These conditions present with variable disease severity and diagnosis may be delayed into adulthood. We report a case of a mother-daughter pair with CRS refractory to maximal medical management. The patients were further evaluated and found to have features consistent with CF, PID, and PCD. All 3 are rare disorders and thought to cause CRS in isolation. Patients with refractory CRS should be further evaluated to identify alternative diagnoses and ensure proper management. Refractory CRS may be multifactorial, with different risk factors simultaneously contributing to its persistence.

Cite

CITATION STYLE

APA

Dorling, M., Hernaiz-Leonardo, J. C., Pascual, A., Nagy, A., & Javer, A. (2024). Short Cilia, Immunodeficiency, and Cystic Fibrosis in a Mother-Daughter Pair. Ear, Nose and Throat Journal. https://doi.org/10.1177/01455613241261563

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free