Medical dictionary. 2011.
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
