HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Correlation of the recurrent FBN1 mutation (c.364C>T) with a unique phenotype in a Chinese patient with Marfan syndrome.

AbstractPURPOSE:
To describe a Chinese patient with Marfan syndrome who had a unique phenotype and a recurrent mutation in the fibrillin-1 (FBN1) gene.
CASE AND METHODS:
A 31-year-old man who had a spontaneous bilateral lens dislocation into the vitreous cavity in childhood was found to have retinal and choroidal detachments in both eyes. A congenital atrial septal defect was detected. Pars plana vitrectomy, lensectomy, and silicone oil tamponade were performed on his right eye. Genomic DNA was extracted from leukocytes of peripheral blood, and the 65 exons and flanking intronic sequences of the FBN1 gene were amplified by polymerase chain reaction for mutational screening.
RESULTS:
A recurrent mutation, c.364C>T was detected in exon 4 that resulted in p.Arg122Cys. The visual acuity of the right eye improved to 6/60 one year after the surgeries.
CONCLUSION:
DNA screening helps in the diagnosis of Marfan syndrome with unique phenotypes. The mutation c.364C>T can be considered to be a hotspot for Marfan patients with predominant ectopia lentis.
AuthorsChongfei Jin, Ke Yao, Zhaohui Sun, Renyi Wu
JournalJapanese journal of ophthalmology (Jpn J Ophthalmol) 2008 Nov-Dec Vol. 52 Issue 6 Pg. 497-499 ISSN: 1613-2246 [Electronic] Japan
PMID19089573 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • FBN1 protein, human
  • Fibrillin-1
  • Fibrillins
  • Microfilament Proteins
  • Cytosine
  • Arginine
  • Cysteine
  • Thymine
Topics
  • Adult
  • Arginine
  • Asian People (genetics)
  • Choroid Diseases (complications, physiopathology, surgery)
  • Cysteine
  • Cytosine
  • Exons
  • Fibrillin-1
  • Fibrillins
  • Heart Septal Defects, Atrial (complications)
  • Humans
  • Lens Subluxation (complications, physiopathology, surgery)
  • Male
  • Marfan Syndrome (complications, genetics)
  • Microfilament Proteins (genetics)
  • Mutation
  • Phenotype
  • Retinal Detachment (complications, physiopathology, surgery)
  • Thymine
  • Time Factors
  • Visual Acuity

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: