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  3. Research By Disease

Disease: Arrhinia

  • A Clinical Report of the Complete Nasal Agenesis: Reconstruction of Congenital Arhinia and Review of the Literature
  • Bosma Arhinia Microphthalmia Syndrome (BAMS): First Report from Vietnam
  • Cholesterol biosynthesis modulates differentiation in murine cranial neural crest cells
  • Congenital arhinia - First published case in Malaysia
  • Congenital arrhinia: A case report and literature review
  • Congenital bilateral anterior nasal atresia in 16 half-sibling Holstein-Friesian calves
  • Congenital complete arhinia with alobar holoprosencephaly
  • Congenital Heminasal Aplasia: Clinical Picture, Radiological Findings, and Follow-up After Early Surgical Intervention
  • DUX4 double whammy: The transcription factor that causes a rare muscular dystrophy also kills the precursors of the human nose
  • Nasal Construction in Congenital Arhinia Due to Novel SMCHD1 Gene Variant
  • Nasal Reconstruction Using a Customized Three-Dimensional-Printed Stent for Congenital Arhinia: Three-Year Follow-up
  • Partial congenital arrhinia: never seen before adult presentation
  • Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations
  • Reconstruction of Congenital Arhinia With Stereolithographic Modeling: Case Correlate and Literature Review
  • The arrhinias: Proboscis lateralis literature review and surgical update
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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