Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations

Samankaltaisia teoksia

• LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma
  Tekijä: Désir, Julie, et al.
  Julkaistu: (2010)
• Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis)
  Tekijä: Khan, Arif O., et al.
  Julkaistu: (2015)
• Spontaneous onset pseudophakic malignant glaucoma secondary to zonular weakness and cilio-lenticular block
  Tekijä: Wilde, Craig, et al.
  Julkaistu: (2018)
• Objective classification of zonular weakness based on lens movement at the start of capsulorhexis
  Tekijä: Yaguchi, Saori, et al.
  Julkaistu: (2017)
• Null Mutations in LTBP2 Cause Primary Congenital Glaucoma
  Tekijä: Ali, Manir, et al.
  Julkaistu: (2009)