1.Experience and procedure of the model of rat heterotopic heart transplantation
Guohua GAI ; Zhendong SUN ; Feng QI ; Jiaji LEI ; Liwei DIAO ; Qinghua ZHANG ; Naishi WU
Journal of Chinese Physician 2012;14(2):182-184
ObjectiveTo summarize the method and experience of the model of rat heterotopic heart transplantation and to improve the rate of success of the experiment.Methods120 heterotopic heart transplantations were performed by Ono's way,including 60 prepared transplantations and 60 formal transplantations.ResultsRate of success of prepared transplantations was 45%,and formal transplantation was 85%.Mean time of formal operation was (74.3±17.1)min,removal time of the donor heart was (7.9±4.2)min,ischemia time was (29.6±10.3) min and the survival time of allograft was (11.1±5.7)days.5 of the recipients had a long-term survival,and the maximum weight was 740 g.ConclusionsGood surgical technique and rigorous perioperative management is very important in setting up the rat model of heterotopic heart transplantation.
2.Surgical management of vertebral sarcoidosis.
Jing LI ; Jingying GAI ; Xiaobin WANG ; Guohua LU ; Bing WANG ; Chang LU
Journal of Central South University(Medical Sciences) 2011;36(9):895-898
OBJECTIVE:
To investigate the clinical characteristics, diagnostic foundation and treatment of vertebral sarcoidosis.
METHODS:
The clinical data of 13 patients with vertebral sarcoidosis who received anterior debridement and instrumentation were retrospectively analyzed.
RESULTS:
The onset of progressive pain in the pathological region was common in the 13 patients. Neurologic deficit existed in 4 cases. Radiographic study showed multiple vertebral bone destructions, and no other systemic lesions were found. Surgical indications were progressive vertebral destruction, spinal instability or neurological deficit. Anterior vertebra resection, and autologous bone grafts fusion with internal fixation were done. No operative mortality and major complications occurred. Diagnosis was confirmed in all patients by pathological exam. After the surgery, metacortandracin treatment was given routinely for 1 year. Patients were followed up for 12-52 (median 26) months, and pain and neurological symptoms were alleviated. Visual analog scale (VAS) score was 7-10 (median 8) points preoperatively, which dropped to 0-4 (median 2) points postoperatively. All patients showed successful bone fusion with no recurrence.
CONCLUSION
For vertebral sarcoidosis associated with progressive instability and/or neurological symptoms, surgical intervention combined with steroid therapy is safe and effective.
Adolescent
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Adult
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Female
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Humans
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Ilium
;
transplantation
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Infusions, Spinal
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Lumbar Vertebrae
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surgery
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Male
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Middle Aged
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Prednisone
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therapeutic use
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Retrospective Studies
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Sarcoidosis
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surgery
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Spinal Diseases
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surgery
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Young Adult
3.Diagnosis of a case with oculocutaneous albinism type Ⅲ with next generation exome capture sequencing.
Yuqiang LYU ; Jing HUANG ; Kaihui ZHANG ; Guohua LIU ; Min GAO ; Zhongtao GAI ; Yi LIU
Chinese Journal of Medical Genetics 2017;34(1):73-77
OBJECTIVETo explore the clinical and genetic features of a Chinese boy with oculocutaneous albinism.
METHODSThe clinical features of the patient were analyzed. The DNA of the patient and his parents was extracted and sequenced by next generation exome capture sequencing. The nature and impact of detected mutation were predicted and validated.
RESULTSThe child has displayed strabismus, poor vision, nystagmus and brown hair. DNA sequencing showed that the patient has carried compound heterozygous mutations of the TYRP1 gene, namely c.1214C>A (p.T405N) and c.1333dupG, which were inherited from his mother and father, respectively. Neither mutation was reported previously.
CONCLUSIONThe child has suffered from oculocutaneous albinism type Ⅲ caused by mutations of the TYRP1 gene.
Albinism, Oculocutaneous ; diagnosis ; genetics ; Amino Acid Sequence ; Base Sequence ; Child, Preschool ; Exome ; genetics ; Family Health ; Female ; Heterozygote ; High-Throughput Nucleotide Sequencing ; methods ; Humans ; Male ; Membrane Glycoproteins ; genetics ; Mutation ; Oxidoreductases ; genetics ; Parents