Axenfeld anomaly

Axenfeld anomaly
a developmental anomaly consisting of posterior embryotoxon and iris processes to the Schwalbe ring. Called also arcus juvenilis and posterior embryotoxon. See also anterior chamber cleavage syndrome, under syndrome.

Medical dictionary. 2011.

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  • Axenfeld anomaly syndrome — Ax·en·feld anomaly, syndrome (ahkґsən felt″) [Theodor Axenfeld, German ophthalmologist, 1867–1930] see under anomaly and syndrome …   Medical dictionary

  • Axenfeld syndrome — Axenfeld anomaly accompanied by glaucoma and defective development of the corneoscleral trabecular meshwork and other angle structures. See also anterior chamber cleavage s …   Medical dictionary

  • Axenfeld — n. Axenfeld anomaly, congenital disorder characterized by hypoplasia of thickening and anterior displacement of Schwalbe s line with iris stromal processes to this line …   English contemporary dictionary

  • Axenfeld syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 30800 ICD10 = ICD9 = ICD9|743.44 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Axenfeld syndrome (also known as Axenfeld Rieger syndrome or Hagedoom syndrome) is the… …   Wikipedia

  • anomalía de Axenfeld — Eng. Axenfeld s anomaly Ver síndrome de Axenfeld …   Diccionario de oftalmología

  • posterior embryotoxon — Axenfeld anomaly …   Medical dictionary

  • anterior chamber cleavage syndrome — a term for several types of mesenchymal dysgenesis affecting neural crest derivatives in the iris, trabecula, and cornea. In ascending severity these disorders are: Axenfeld anomaly, Axenfeld syndrome, Rieger anomaly, and Rieger syndrome …   Medical dictionary

  • arcus juvenilis — 1. a. corneae. 2. Axenfeld anomaly …   Medical dictionary

  • Forkhead box C1 — Forkhead box C1, also known as FOXC1, is a human gene.cite web | title = Entrez Gene: FOXC1 forkhead box C1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2296| accessdate = ] PBB Summary section title =… …   Wikipedia

  • PITX2 — Paired like homeodomain transcription factor 2, also known as PITX2, is a human gene. PBB Summary section title = summary text = This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins.… …   Wikipedia

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