HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Molecular genetics of Chinese families with TGFBI corneal dystrophies.

AbstractPURPOSE:
To identify clinical features and mutations within the transforming growth factor-beta-induced (TGFBI) gene in three Chinese families with Granular corneal dystrophy, type 1 (GCD1) and Granular corneal dystrophy, type 2 (GCD2).
METHODS:
Clinical features of GCD1 and GCD2 in three Chinese families were studied with slit-lamp and in vivo laser scanning confocal microscopy (LSCM). Molecular genetic analysis was performed on nine patients and fifteen unaffected individuals from these families. All exons of TGFBI were amplified by polymerase chain reaction (PCR) and sequenced.
RESULTS:
Morphological changes in the cornea among affected individuals from three Chinese families examined by in vivo LSCM were almost the same. A heterozygous mutation C>T (R555W) was identified in exon 12 of TGFBI in patients of family A with GCD1. Another heterozygous mutation G>A (R124H) was found in exon 4 of TGFBI in affected members of family B and C with GCD2.
CONCLUSIONS:
Mutations R555W and R124H in TGFBI were identified in three Chinese families with GCD. Even though there are a variety of mutations in TGFBI of GCD, the different subtypes of GCD (GCD1, GCD2, and GCD3) are in fact the same disorder. Our work supports the hypothesis that corneal dystrophies with the common genetic basis in TGFBI should be grouped together as TGFBI corneal dystrophies.
AuthorsTing Zhang, Naihong Yan, Wenhan Yu, Yun Liu, Guo Liu, Xiaomei Wu, Jinxian Lian, Xuyang Liu
JournalMolecular vision (Mol Vis) Vol. 17 Pg. 380-7 (Feb 04 2011) ISSN: 1090-0535 [Electronic] United States
PMID21311742 (Publication Type: Journal Article)
Chemical References
  • Transforming Growth Factor beta1
Topics
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Child
  • Child, Preschool
  • China
  • Corneal Dystrophies, Hereditary (ethnology, genetics)
  • Exons
  • Female
  • Heterozygote
  • Humans
  • Male
  • Microscopy, Confocal (methods)
  • Middle Aged
  • Models, Genetic
  • Mutation
  • Pedigree
  • Polymerase Chain Reaction
  • Transforming Growth Factor beta1 (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: