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Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous.

AuthorsA Arikawa, S Yoshida, H Yoshikawa, K Ishikawa, Y Yamaji, R-I Arita, A Ueno, T Ishibashi
JournalEye (London, England) (Eye (Lond)) Vol. 24 Issue 2 Pg. 391-3 (Feb 2010) ISSN: 1476-5454 [Electronic] England
PMID19461663 (Publication Type: Case Reports, Letter)
Chemical References
  • Homeodomain Proteins
  • Transcription Factors
Topics
  • Abnormalities, Multiple (genetics)
  • Anterior Chamber (pathology)
  • Cataract (genetics, pathology)
  • Cataract Extraction
  • Cornea (pathology)
  • Glaucoma (congenital, genetics, pathology, surgery)
  • Homeodomain Proteins (genetics)
  • Humans
  • Infant, Newborn
  • Iris (pathology)
  • Male
  • Mutation
  • Transcription Factors (genetics)
  • Treatment Outcome
  • Vitrectomy
  • Vitreous Body (abnormalities, pathology)
  • Homeobox Protein PITX2

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