Familial nasal acilia
| Familial nasal acilia | |
|---|---|
| Other names | Familial nasal acilia syndrome |
Genetic mutation | |
| Prevention | None |
| Prognosis | Medium |
| Frequency | rare |
| Deaths | - |
Familial nasal acilia is a rare
dyspnea, lobar atelectasis, bronchiectasis and neo-natal pneumonia. Other symptoms that occur later in life include chronic moist coughing, chronic sinusitis, chronic otitis media, chronic rhinitis, and recurrence of upper and lower respiratory tract infections.[1][2]
Exact prevalence is unknown,
OrphaNet estimates this condition to affect less than 1 out of every million people worldwide.[3] R Soferman et al. described this disorder to be "autosomal recessive".[4][5]
References
- ^ "Familial nasal acilia - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 18 July 2022.
- ^ Peña, Yanin (27 October 2017). "Acilia nasal familiar – FEMEXER" (in Spanish). Retrieved 18 July 2022.
- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Familial nasal acilia". www.orpha.net. Retrieved 18 July 2022.
{{cite web}}: CS1 maint: numeric names: authors list (link) - PMID 8813877.
- PMID 8813877.
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