1.A cases of velamentous insertion of umbilical cord.
Ho Sang SEO ; Sam Hyeon CHO ; Soo Hyeon JO ; Kyeong Tae KIM ; Yoon Yeong HWANG ; Jai Euk LEE
Korean Journal of Obstetrics and Gynecology 1993;36(12):3970-3975
No abstract available.
Umbilical Cord*
2.Sperm-specific Cation Channels, CatSper Family; Characteristics, Function, and Clinical Value.
Yeong Jin CHOI ; Kang Woo CHEON ; Ju Tae SEO
Korean Journal of Andrology 2006;24(1):1-7
In human reproduction, fertilization is the first step for successful pregnancy. From the perspective of sperm physiology, the progressive motility and capacitation, including hyperactivation and acrosome reaction, are the most important factors in the fertilization of oocytes. Numerous studies have demonstrated the roles of calcium ions, cyclic nucleotides, and bicarbonate in the acquisition of progressive motility and capacitation. Among these factors, calcium ion plays the most important role. Sperm possess several calcium channels, including voltage-gated calcium channel, cyclic nucleotide-gated calcium channel, transient receptor potential channel, and channels of the CatSper family The CatSper family is a newly-identified group of four sperm-specific cation channels. CatSper1 and CatSper2 proteins localize on the sperm tail and play a critical role in sperm motility and fertilization. In contrast, CatSper3 and CatSper4 proteinsare expressed only in the acrosomal region of sperm head, which implies that they may have a role in the acrosome reaction. Taken together, the CatSper family is the most important group of calcium channels for regulating sperm physiology and appear to be an attractive target for non-hormonal male contraceptives.
Acrosome Reaction
;
Calcium
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Calcium Channels
;
Contraceptive Agents, Male
;
Fertilization
;
Humans
;
Ions
;
Nucleotides, Cyclic
;
Oocytes
;
Physiology
;
Pregnancy
;
Reproduction
;
Sperm Head
;
Sperm Motility
;
Sperm Tail
;
Spermatozoa
4.Temporomandibular Joint Segmentation Using Deep Learning for Automated Three-Dimensional Reconstruction
Young-Tae CHOI ; Ho-Jun SONG ; Jae-Seo LEE ; Yeong-Gwan IM
Journal of Oral Medicine and Pain 2024;49(4):109-117
Purpose:
Cone beam computed tomography (CBCT) is widely used to evaluate the temporomandibular joint (TMJ). For the three-dimensional (3D) assessment of the TMJ, segmentation of the mandibular condyle and articular fossa is essential. This study aimed to perform deep learning-based 3D segmentation of the mandibular condyle on CBCT images and evaluate the performance of the segmentation.
Methods:
CBCT scan data from 99 patients (mean age: 53.3±19.2 years) diagnosed with TMJ disorders were analyzed. From the CBCT images, sagittal, coronal, and axial planes showing the mandibular condyle were selected and combined to form two-dimensional (2D) images. The U-Net deep learning model was used to exclusively segment the mandibular condyle area from the 2D images. From these results, 3D images of the mandibular condyle were reconstructed. Accuracy, precision, recall, and the Dice coefficient were calculated to appraise segmentation performance in each plane.
Results:
The average Dice coefficient was 0.92 for the coronal and axial planes and 0.82 for the sagittal plane. The CBCT image-based segmentation performance of the mandibular condyle in the coronal and axial planes exceeded that in the sagittal plane. The sharpness and uniformity of the 2D images affected segmentation performance, with segmentation errors more likely occurring in non-uniform images. Certain segmentation errors were corrected through software processing. Finally, the segmented mandibular condyle images were applied to the CBCT data to reconstruct a 3D TMJ model.
Conclusions
Mandibular condyle 3D segmentation on CBCT images using U-Net may help evaluate and diagnose TMJ disorders. The proposed segmentation method may assist clinicians in efficiently analyzing CBCT images, particularly in cases involving anatomical abnormalities.
5.Analysis of Missed Fractures by Bone Scan in Elderly Hip Fracture Patients with Osteoporosis
Tae Hun LEE ; Yeong Hyun LEE ; Seo Won KANG
Journal of the Korean Fracture Society 2024;37(3):144-149
Purpose:
The incidence of hip fractures is increasing due to an increase in elderly populations because elderly patients often have accompanying diseases, such as cognitive impairment or dementia, which may lead to missed fractures. Therefore, this study assessed the utility of bone scans in detecting missed fractures in elderly patients.
Materials and Methods:
This study analyzed the data from 178 patients treated from January 2014 to March 2023. The inclusion criteria were patients who had hip fractures with osteoporosis over 70 years old. Bone scans were performed on average 10 days after injury. The rate and trend of missed fractures not detected in the initial diagnosis were determined based on sex, age, dementia status, and the presence of osteoporosis.
Results:
Among the 178 hip fracture patients over 70 years old, 37 patients had a history of being diagnosed with dementia, and 141 patients had never been diagnosed. Missed fractures were confirmed in 49 cases (42 patients) (23.6%). The dementia group had 13 missed fractures, and the non-dementia group had 36 missed fractures, but there was no significant difference. Rib fractures were most common, followed by vertebral fractures.
Conclusion
Missed diagnoses of fractures were common among elderly hip fracture patients. A whole body bone scan appeared to be effective in detecting missed fractures. Therefore, identifying accompanying fractures through bone scans and delivering appropriate treatment can play an important role in postoperative rehabilitation.
6.Factors Affecting Fatigue in Patients with Type II Diabetes Mellitus in Korea.
Yeong Mi SEO ; Jong Ryeal HAHM ; Tae Kyung KIM ; Won Hee CHOI
Asian Nursing Research 2015;9(1):60-64
PURPOSE: This study aimed to characterize and identify the factors affecting fatigue in patients with type II diabetes mellitus in Korea. METHODS: A total of 180 patients with type II diabetes mellitus were recruited from the outpatient clinic of a tertiary care hospital. For data collection, a questionnaire survey of diabetes history, hypoglycemia symptoms, and fatigue was conducted between January and February 2011. Data were analyzed using t test, analysis of variance, Pearson's correlation, and hierarchical multiple regression. RESULTS: The mean fatigue and hypoglycemia symptom scores of patients with type II diabetes mellitus were 2.88 +/- 0.61 and 6.18 +/- 12.60, respectively. Hypoglycemia symptoms (p = .004), disease duration (p < .001), and age (p < .001) correlated positively with fatigue. Hierarchical multiple regression analysis revealed that hypoglycemia symptoms was the variable positively influencing fatigue in patients with type II diabetes mellitus after adjustment for influences of demographic and clinical characteristic variables. CONCLUSIONS: Hypoglycemia symptoms were confirmed to be a predictor of fatigue. Consequently, it is essential to consider age, and disease duration as well as hypoglycemia symptoms to intervene fatigue effectively among patients with type II diabetes mellitus.
Adult
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Aged
;
Aged, 80 and over
;
Analysis of Variance
;
Cross-Sectional Studies
;
Diabetes Mellitus, Type 2/complications/*epidemiology
;
Fatigue/complications/*epidemiology
;
Female
;
Humans
;
Hypoglycemia/complications/*epidemiology
;
Male
;
Middle Aged
;
Regression Analysis
;
Republic of Korea/epidemiology
;
Retrospective Studies
;
Risk Factors
;
Surveys and Questionnaires
;
Young Adult
7.Outcome of Preimplantation Genetic Diagnosis in Patients with Klinefelter Syndrome.
Jin Yeong KIM ; Chun Kyu LIM ; Jin Hyun JUN ; So Yeon PARK ; Ju Tae SEO ; Sun Hwa CHA ; Mi Kyoung KOONG ; Inn Soo KANG
Korean Journal of Fertility and Sterility 2004;31(4):253-260
OBJECTIVES: Klinefelter syndrome is the most common genetic cause of male infertility and presents with 47, XXY mainly or 46, XX/47, XXY mosaicism. It is characterized by hypogonadism and azoospermia due to testicular failure, however, sporadic cases of natural pregnancies have been reported. With the development of testicular sperm extraction (TESE) and intracytoplasmic sperm injection (ICSI), sperm can be retrieved successfully and ART is applied in these patients for pregnancy. It has been suggested that the risk of chromosome aneuploidy for both sex chromosome and autosome is increased in the sperms from 47, XXY germ cells. Considering the risk for chromosomal aneuploidy in the offspring, preimplantation genetic diagnosis (PGD) could be applied as a safe and more effective treatment option in Klinefelter syndrome. The aim of this study is to assess the outcome of PGD cycles by using FISH for sex chromosome and autosome in patients with Klinefelter syndrome. MATERIALS AND METHODS: From Jan. 2001 to Dec. 2003, PGD was attempted in 8 cases of Klinefelter syndrome but TESE was failed to retrieve sperm in the 3 cases, therefore PGD was performed in 8 cycles of 5 cases (four 47, XXY and one 46, XY/47, XXY mosaicism). In one case, ejaculated sperm was used and in 4 cases, TESE sperm was used for ICSI. After fertilization, blastomere biopsy was performed in 6~10 cell stage embryo and the chromosome aneuploidy was diagnosed by using FISH with CEP probes for chromosome X, Y and 17 or 18. RESULTS: A total of 127 oocytes were retrieved and ICSI was performed in 113 mature oocytes. The fertilization rate was 65.3+/-6.0% (mean+/-SEM) and 76 embryos were obtained. Blastomere biopsy was performed in 61 developing embryos and FISH analysis was successful in 95.1% of the biopsied blastomeres (58/61). The rate of balanced embryos for chromosome X, Y and 17 or 18 was 39.7+/-6.9%. The rate of aneuploidy for sex chromosome (X and Y) was 45.9+/-5.3% and 43.2+/-5.8% for chromosome 17 or 18, respectively. Embryo transfer was performed in all 8 cycles and mean number of transferred embryos was 2.5+/-0.5. In 2 cases, clinical pregnancies were obtained and normal 46, XX and 46, XY karyotypes were confirmed by amniocentesis, respectively. Healthy male and female babies were delivered uneventfully at term. CONCLUSION: The patients with Klinefelter syndrome can benefit from ART with TESE and ICSI. Considering the risk of aneuploidy for both sex chromosome and autosome in the sperms and embryos of Klinefelter syndrome, PGD could be offered as safe and more effective treatment option.
Amniocentesis
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Aneuploidy
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Azoospermia
;
Biopsy
;
Blastomeres
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Chromosomes, Human, Pair 17
;
Embryo Transfer
;
Embryonic Structures
;
Female
;
Fertilization
;
Germ Cells
;
Humans
;
Hypogonadism
;
Infertility, Male
;
Karyotype
;
Klinefelter Syndrome*
;
Male
;
Mosaicism
;
Oocytes
;
Pregnancy
;
Preimplantation Diagnosis*
;
Prostaglandins D
;
Sex Chromosomes
;
Sperm Injections, Intracytoplasmic
;
Spermatozoa
8.Actinobacillus actinomycetemcomitans Indeces Apoptosis of Jurkat Cell Line Through the Cleavage of Poly (ADP-ribose) Polymerase.
Sang Hwa LEE ; Su Yeong SEO ; Su Jin JEONG ; Seung Ho YOO ; Sun Mee PARK ; Min Ho JEONG ; Sung Tae YEE ; Jung Man KIM
Journal of the Korean Society for Microbiology 1998;33(5):507-519
No abstract available.
Actinobacillus*
;
Aggregatibacter actinomycetemcomitans*
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Apoptosis*
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Humans
;
Jurkat Cells*
9.Progressive Supranuclear Palsy-Like Syndrome after Surgical Repair of Chronic Ascending Aorta Dissection.
Chang Hwan RYU ; Seok Jae KANG ; Yeong Seo KIM ; Hee Tae KIM
Journal of the Korean Neurological Association 2016;34(5):363-366
A 70-year-old woman underwent cardiopulmonary bypass surgery for aorta dissection. After 10 days she developed a vertical gaze palsy, and 2 months later she presented with dysarthria, bradykinesia, postural instability, blepharospasm, and truncal tilt to the left. Brain imaging indicated old lacunes in the bilateral thalamus. Her symptoms remained unchanged during a 4-year follow-up, which seems to be incompatible with progressive supranuclear palsy (PSP). However, the clinical features of this case were suggestive of PSP-like syndrome after cardiopulmonary bypass surgery.
Aged
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Aorta*
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Blepharospasm
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Cardiopulmonary Bypass
;
Dysarthria
;
Female
;
Follow-Up Studies
;
Humans
;
Hypokinesia
;
Neuroimaging
;
Paralysis
;
Parkinsonian Disorders
;
Supranuclear Palsy, Progressive
;
Thalamus
10.IgA Nephropathy: Correlation of WHO Classification and Morphologic Semi-quantitative Scoring System.
Kyung Jin SEO ; Tae Jung KIM ; Kyo Young LEE ; Sang In SHIM ; Yeong Jin CHOI
Korean Journal of Pathology 2009;43(3):244-249
BACKGROUND: IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide, and the clinical course of IgAN shows marked variability. Many efforts have made to histologically predict the clinical outcome. There are two methods to classify IgAN. One is mainly based on the glomerular changes, such as the WHO and the Lee and Haas classification systems. The other is a morphologic semi-quantitative scoring system, which counts the changes of the glomerular, tubulointerstitial and vascular structures, respectively. The purpose of this study is to determine whether the WHO classification properly reflects the various morphologic findings of IgAN. METHODS: We analyzed 354 cases of IgAN by both the WHO classification system and the semiquantitative scoring system and evaluated the correlations of these two methods. RESULTS: The severity of the glomerular lesions (glomerulosclerosis, capsular adhesion and mesangial matrix expansion) and the tubulointerstitial lesions (interstitial fibrosis, tubular atrophy and interstitial lymphocytic infiltration) are strongly correlated with the increase of the WHO classes of IgAN (Spearman's rho [R] > or =0.5, p<0.05). There is a weak correlation between crescent formation and the increase of the WHO classes (R=0.3, p<0.05). CONCLUSIONS: This study shows that the WHO classification well reflects the severity of various morphologic findings and this suggests a complementary role for the semi-quantitative scoring system in classifying IgAN.
Atrophy
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Fibrosis
;
Glomerulonephritis
;
Glomerulonephritis, IGA
;
Immunoglobulin A