1.Clinical effects of mixed baggy eyelid plasty with a new myocutaneous flap method combined middle face lifting
Qigang ZHU ; Yanlong XU ; Rong SUN ; Zhiming WANG
Chinese Journal of Medical Aesthetics and Cosmetology 2017;23(4):259-261
Objective To evaluate the postoperative effects of mixed baggy eyelid plasty with a new myocutaneous flap method combined with middle face lifting.Methods It was a retrospective study of old patients with skin and/or orbicular muscle relaxation eyelid bulging.28 patients were the control group with mixed baggy eyelid plasty with a new myocutaneous flap method only,and 32 cases were the observation group with combined middle face lift method.After six months,the condition of postoperative recovery,degree of satisfaction and complications were compared between two groups with a detailed statistical analysis.Results After six months,the total effective rate of the observation group was 96.88%,higher than the control group (92.85%).The total incidence of complications of the observation group was 3.13%,lower than the other group (7.14%).The total satisfactory rate of the observation group was 93.75%,higher than the control group (89.29%).The differences of two groups were all statistically significant (P<0.05).Conclusions The advantages of mixed baggy eyelid plasty with a new myocutaneous flap combined middle face lifting method are more effectively facial aging improved and higher satisfaction than others.
2.Correction of upper eyelid depression by transposition of orbital septum fat.
Qingyang LIU ; Shuya PAN ; Da CHEN ; Qigang ZHU ; Yilan SONG ; Jiting QIU ; Xinwen GUO
Chinese Journal of Plastic Surgery 2015;31(2):100-102
OBJECTIVETo discuss the operation method and characteristic of correcting upper eyelid depression by transposition of orbital septum fat.
METHODSDuring the double eyelid surgery, we set.the lateral orbital septum fat completely free, while the bottom is still connected with the middle orbital septum fat. We separate a tunnel from the middle to the inner side in orbital septum, and the separated orbital septum fat is transposed to the inner side of orbital septum by the tunnel with suturing fixation.
RESULTSFrom March 2008 to October 2013, 51 cases with upper eyelid depression were treated successfully. Patients were followed up for 3 months to 3 years (average, 7. 5 months) with sustained aesthetic results.
CONCLUSIONSOrbital septum fat transposition can successfully correct the upper eyelid depression. It should become a regular procedure in blepharoplasty.
Adipose Tissue ; transplantation ; Blepharoplasty ; methods ; Esthetics ; Eyelids ; abnormalities ; surgery ; Humans ; Orbit
3.Detection of a patient with ring chromosome 15 by low-coverage massively parallel copy number variation sequencing.
Qiong PAN ; Li ZHANG ; Fengting ZHANG ; Xin JIN ; Yue HU ; Liyan ZHU ; Longfei CHENG ; Qigang ZHANG ; Ying NING
Chinese Journal of Medical Genetics 2017;34(3):406-410
OBJECTIVETo explore the genetic cause for a child with developmental delay.
METHODSThe karotypes of the child and her parents were analyzed with G-banding analysis. Their genome DNA was analyzed with low-coverage massively parallel copy number variation sequencing (CNV-seq) and verified by single nucleotide polymorphism array (SNP-array).
RESULTSThe karyotype of the child was ascertained as 46,XX,r(15)(p13q26.3), while both parents showed a normal karyotype. CNV-seq and SNP-array have identified a de novo 15q26.2-q26.3 deletion in the child with a size of approximately 3.60 Mb.
CONCLUSIONThe abnormal phenotype of the patient carrying the ring chromosome 15 may be attributed to the presence of the 15q26.2-q26.3 microdeletion. The deletion and haploinsufficiency of the IGF1R gene probably underlie the main clinical features of the patient.
Child, Preschool ; Chromosome Banding ; Chromosomes, Human, Pair 15 ; genetics ; DNA Copy Number Variations ; Female ; Humans ; Karyotyping ; Mosaicism ; Ring Chromosomes ; Sequence Deletion
4.Analysis of clinical manifestation and genetic mutations in two patients with Cornelia de Lange syndrome.
Yequan MIAO ; Yueyue ZHU ; Qigang ZHANG ; Haowei GUO ; Yuxiang ZHAO ; Longfei CHENG ; Liangrong HAN ; Ying NING ; Qiong PAN
Chinese Journal of Medical Genetics 2018;35(4):493-497
OBJECTIVETo detect potential mutations in two neonates suspected for Cornelia de Lange syndrome (CdLS).
METHODSPeripheral blood samples from the neonates and their parents were collected and analyzed for CdLS-related genes using targeted sequence capture and next-generation sequencing. Suspected mutations were confirmed by direct Sanger sequencing.
RESULTSThe neonates were found to respectively carry mutations c.7219C to T and p.D2339Lfs*4 of the NIPBL gene, among which the p.D2339Lfs*4 mutation has not been reported previously. No pathogenic mutation was found in other CdLS-related genes including NIPBL, SMC1A, SMC3, RAD21 and HDAC8.
CONCLUSIONThe c.7219C to T and p.D2339Lfs*4 mutations of the NIPBL gene probably account for the disease in both patients.