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Congenital Arhinia: A Neonatal Case Report.
Kolsi, Nadia; Mekki, K; Regaieg, Ch; Ben Hamed, A; Charfi, M; Bouraoui, A; Gargouri, A; BenThabet, A; Hentati, N.
Affiliation
  • Kolsi N; Faculty of Medicine, University of Sfax, Sfax, Tunisia.
  • Mekki K; Neonatology Department, Hedi Chaker Hospital, Sfax, Tunisia.
  • Regaieg C; Faculty of Medicine, University of Sfax, Sfax, Tunisia.
  • Ben Hamed A; Neonatology Department, Hedi Chaker Hospital, Sfax, Tunisia.
  • Charfi M; Faculty of Medicine, University of Sfax, Sfax, Tunisia.
  • Bouraoui A; Neonatology Department, Hedi Chaker Hospital, Sfax, Tunisia.
  • Gargouri A; Faculty of Medicine, University of Sfax, Sfax, Tunisia.
  • BenThabet A; Neonatology Department, Hedi Chaker Hospital, Sfax, Tunisia.
  • Hentati N; Faculty of Medicine, University of Sfax, Sfax, Tunisia.
Ear Nose Throat J ; : 1455613231185038, 2023 Jul 21.
Article in En | MEDLINE | ID: mdl-37480254
ABSTRACT
Congenital arhinia or nasal absence is a rare condition, with only less than 100 cases published in the literature to date. It is a rare condition that causes respiratory distress during the neonatal period. Although stabilization of the airway is the priority, management is not clearly defined, given the rarity of the malformation. We report a case of arhinia in a female newborn and briefly review the literature.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ear Nose Throat J Year: 2023 Document type: Article Affiliation country: Túnez

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ear Nose Throat J Year: 2023 Document type: Article Affiliation country: Túnez