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1.
Chinese Journal of Plastic Surgery ; (6): 48-50, 2007.
Article in Chinese | WPRIM | ID: wpr-297099

ABSTRACT

<p><b>OBJECTIVE</b>We have studied 4 generations 12 patients in a family which has blepharophimosis-ptosis-epicanthus-inversus syndrome (BPES) for the gene, FOXL2, the group also have 12 normal members in this family and other 80 normal individuals for contrast.</p><p><b>METHODS</b>The FOXL2 gene was amplified by polymerase chain reaction and then analyzed by direct genomic sequencing.</p><p><b>RESULTS</b>A 892C > T at nucleotides in FOXL2 was found in the twelve affected patients. No mutations was found in any of the health members in the family.</p><p><b>CONCLUSIONS</b>FOXL2 may be a important pathogenesis for the disease in this Chinese family.</p>


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Young Adult , Asian People , Genetics , Blepharophimosis , Ethnology , Genetics , Forkhead Box Protein L2 , Forkhead Transcription Factors , Genetics , Genotype , Mutation , Pedigree , Phenotype , Sequence Analysis, DNA , Syndrome
2.
Journal of Shanghai Jiaotong University(Medical Science) ; (6)2006.
Article in Chinese | WPRIM | ID: wpr-640535

ABSTRACT

0.05).The survival area and capillary density were more favorable in the EPCs-injection sites than the controls(P

3.
Chinese Journal of Medical Genetics ; (6): 372-375, 2005.
Article in English | WPRIM | ID: wpr-280048

ABSTRACT

<p><b>OBJECTIVE</b>To screen mutations in the forkhead transcriptional factor 2 gene (FOXL2) in six Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome(BPES).</p><p><b>METHODS</b>PCR amplification and direct sequencing of the FOXL2 coding region in genomic DNA were performed in affected patients and 80 healthy controls. BLAST analysis of the sequence was made on Internet.</p><p><b>RESULTS</b>A novel 951-953(delC) was found in the two affected patients of a Chinese family with BPES. No mutations were found in the healthy controls. The 951-953(delC) may cause a frameshift mutation after codon 238 that exists downstream of the forkhead domain, resulting in the production of truncated proteins.</p><p><b>CONCLUSION</b>These findings indicated that the 951-953(delC) deletion mutation in the two patients resulted in truncated proteins and hence led to their BPES. To the authors' knowledge, the 951-953(delC) in FOXL2 has not been previously reported.</p>


Subject(s)
Female , Humans , Male , Amino Acid Sequence , Base Sequence , Blepharophimosis , Genetics , Blepharoptosis , Genetics , China , Eyelid Diseases , Genetics , Family Health , Forkhead Box Protein L2 , Forkhead Transcription Factors , Genetics , Molecular Sequence Data , Mutation , Pedigree , Sequence Alignment
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