Congenital arrhinia: A case report and literature review
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference21 articles.
1. FSHD type 2 and Bosma arhinia microphthalmia syndrome: two faces of the same mutation;Mul;Neurology,2018
2. Nose underdevelopment-etiology, diagnosis and treatment;Fijałkowska;Otolaryngologia polska= The Polish otolaryngology,2016
3. Occurrence of complete arhinia in two siblings with a clinical picture of Treacher Collins syndrome negative for TCOF1, POLR1D and POLR1C mutations;Cesaretti;Clin. Dysmorphol.,2011
4. Bosma arhinia microphthalmia syndrome: clinical report and review of the literature;Brasseur;Am. J. Med. Genet.,2016
5. Familial arhinia, choanal atresia, and microphthalmia;Thiele;Am. J. Med. Genet.,1996
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hemiarhinia caused by a missense variation in SMCHD1: A mild phenotype in the clinical spectrum of Bosma arhinia microphthalmia syndrome;American Journal of Medical Genetics Part A;2024-05-29
2. Dilemmas in the management of lacrimal drainage anomalies in BOSMA (congenital arhinia-microphthalmia) syndrome;Orbit;2024-05-07
3. Imaging of the fetal oral cavity, airway and neck;Pediatric Radiology;2021-05-12
4. Seltene Erkrankungen der Nase, der Nasennebenhöhlen und der vorderen Schädelbasis;Laryngo-Rhino-Otologie;2021-04
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