• Title/Summary/Keyword: Family Report

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A Review of the Family Embolemidae (Hymenoptera: Chrysidoidea) from South Korea

  • Kim, Chang-Jun;Lee, Jong-Wook
    • Animal Systematics, Evolution and Diversity
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    • v.32 no.2
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    • pp.63-71
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    • 2016
  • Previously only one species, Embolemus ruddii Westwood, 1833, of the family Embolemidae has been recorded in South Korea. As part of a recent study of this family, we newly report four species from South Korea: Embolemus hachijoensis Hirashima et Yamagishi, 1975; E. krombeini Olmi, 1996; E. sensitivus Xu, Olmi et Guglielmino, 2012; Ampulicomorpha thauma Rasnitsyn et Matveev, 1989. The genus, Ampulicomorpha Ashmead, 1893, is recorded for the first time in South Korea. Embolemus ruddii was previously recorded from South Korea because considered synonym of E. walkeri. However, in recent years the two species were separated and E. ruddii was considered absent in the far east, where on the contrary E. walkeri is present. Therefore, five species in two genera are now recognized as the South Korean embolemid fauna. A key to the South Korean Embolemidae species is provided.

A Case Study of Familial Scoliosis (가족성 척추측만증(Familial Scoliosis)의 증례보고)

  • Park, Kyung-Moo;Soh, Mun-Gie;Song, Yun-Kyung;Lim, Hyung-Ho
    • Journal of Korean Medicine Rehabilitation
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    • v.18 no.3
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    • pp.187-199
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    • 2008
  • Objectives : The purpose of this study is to report the concept of familial scoliosis through eight cases. Methods : The family tree was constructed with eight cases which was diagnosed idiopathic scoliosis by physical examination and radiological study. Results : According to the family tree of this sibs, idiopathic scoliosis apparently behaves as an autosomal dominant inheritance. As to parents and grandparents, although they are not confirmed the appearance of idiopathic scoliosis, we know that they transmit trait to their descendants as a genotype. Conclusions : This study is shown that idiopathic scoliosis has a familial condition and provided useful information that can be used early diagnosis and treatment with screen tests based on the family tree.

Infant Day-Care and Family Factors on Maternal Behavior (영아보육 및 가족변인이 어머니의 앙육행동에 미치는 영향)

  • 박성연;고은주
    • Journal of the Korean Home Economics Association
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    • v.41 no.7
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    • pp.91-106
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    • 2003
  • Multiple features of infant day-care are explored, including age of entry, quantity, quality and stability of day-care. And relative contribution of day-care and family factors on maternal behaviors are examined. Data were gathered from 299 mothers who have infants aged under 36 months using self-report questionnaires. Results show that more than 40% infants enter day-care before 6 months of their life and about 85% of infants have far more than 30 hours of care a week. Half of the infants experience different day-care arrangements more than once. Compared to the other types of day-care, frequency of day-care arrangement change and quality of care are highest in private child-care centers. A series of Hierarchical regression results reveal that quality of day care is negatively related to mothers' control behavior whereas positively related to mothers' responsive behavior. But in general, family and child characteristics play a greater role in mothers' parenting behaviors than infant day-care characteristics.

Sensorineural Hearing Loss and Wernicke Encephalopathy: A Case Report and Literature Review

  • Ton, Angie Nu;Jethwa, Trisha;Stamper, Greta C;Yenior, Ashley
    • Journal of Audiology & Otology
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    • v.25 no.1
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    • pp.55-58
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    • 2021
  • Sensorineural hearing loss (SNHL) is seldom associated with Wernicke encephalopathy (WE) or thiamine deficiency. While thiamine deficiency and repletion are often considered prior to dextrose infusions in patients with chronic alcohol abuse to prevent WE, they are often overlooked in non-alcoholic patients who are also at risk for malnutrition. In this paper we describe a case of a non-alcoholic 28-year-old female status post-sleeve gastrectomy who developed SNHL in the setting of thiamine deficiency and WE, with ongoing hearing impairment requiring hearing aids despite thiamine repletion.

Sensorineural Hearing Loss and Wernicke Encephalopathy: A Case Report and Literature Review

  • Ton, Angie Nu;Jethwa, Trisha;Stamper, Greta C;Yenior, Ashley
    • Korean Journal of Audiology
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    • v.25 no.1
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    • pp.55-58
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    • 2021
  • Sensorineural hearing loss (SNHL) is seldom associated with Wernicke encephalopathy (WE) or thiamine deficiency. While thiamine deficiency and repletion are often considered prior to dextrose infusions in patients with chronic alcohol abuse to prevent WE, they are often overlooked in non-alcoholic patients who are also at risk for malnutrition. In this paper we describe a case of a non-alcoholic 28-year-old female status post-sleeve gastrectomy who developed SNHL in the setting of thiamine deficiency and WE, with ongoing hearing impairment requiring hearing aids despite thiamine repletion.

First Record of the Family Curtonotidae (Diptera: Ephydroidea) from Korea with One Unrecorded Species

  • Dongmin Kim;Young-Kun Kim;Sang Jae Suh
    • Animal Systematics, Evolution and Diversity
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    • v.40 no.1
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    • pp.16-20
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    • 2024
  • The family Curtonotidae, known as the Hunchbacked or Quasimodo fly, is a small group of acalyptrate flies belonging to the superfamily Ephydroidea. Until now, a total of 103 species under four genera have been recorded worldwide, mainly distributed in tropical and subtropical areas. Among them, only five species of the genus Curtonotum Macquart, 1843 have been recorded in the Palaearctic region, mainly in the Russian Far East, but there are still no previous reports in the Korean fanua. In this study, we firstly report the family Curtonotidae Duda, 1934 from Korea with Curtonotum maritimum Ozerov, 2007. Additionally, we provide taxonomic information and a key for the Palaearctic Curtonotum species.

Factors associated with Health-related Quality of Life among Family Caregivers of Elders Receiving Home Care Services (재가 장기요양노인 가족수발자의 건강 관련 삶의 질 영향요인)

  • Kim, Eun-Young;Yeo, Jung Hee
    • Research in Community and Public Health Nursing
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    • v.23 no.2
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    • pp.117-126
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    • 2012
  • Purpose: The purpose of this study was to identify the factors associated with the health-related quality of life of family caregivers. Methods: A cross-sectional study was conducted. This study included 191 primary family caregivers of elders who used home care services (home-visit nursing, home-visit care, daycare) covered by the public long-term care insurance. Data were collected using self-report questionnaires from December 2010 to June 2011. These data were analyzed by using hierarchical multiple regression. Results: The majority of the family caregivers were female (79.6%) and daughters-in-law (28.8%). The mean depression score was $6.33{\pm}6.49$ and the mean health-related quality of life score was $0.69{\pm}0.39$. It was found that the factors affecting the health-related quality of life of family caregivers included depression (${\beta}$=-.406, p<.001), home-visit nursing use (${\beta}$=.296, p<.001), and daycare use (${\beta}$=.178, p=.015), which accounted for 36.6% of their health-related quality of life. Conclusion: Using home-visit nursing and daycare services has a positive effect on the health-related quality of life of family caregivers. To improve health-related quality of life of family caregivers, South Korea needs to fully activate the home-visit nursing and daycare services, and to strengthen family support programs.

PKD2 interacts with Lck and regulates NFAT activity in T cells

  • Li, Qing;Sun, Xiaoqing;Wu, Jun;Lin, Zhixin;Luo, Ying
    • BMB Reports
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    • v.42 no.1
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    • pp.35-40
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    • 2009
  • Protein kinase D2 (PKD2) is a member of the PKD serine/threonine protein kinase family that has been implicated in the regulation of a variety of cellular processes including proliferation, survival, protein trafficking and immune response. In the present study, we report a novel interaction between PKD2 and Lck, a member of the Src tyrosine protein kinase family that is predominantly expressed in T cells. This interaction involved the C-terminal kinase domains of both PKD2 and Lck. Moreover, co-expression of Lck enhanced the tyrosine phosphorylation of PKD2 and increased its kinase activity. Finally, we report that PKD2 enhanced T cell receptor (TCR)-induced nuclear factor of T cell (NFAT) activity in Jurkat T cells. These results suggested that Lck regulated the activity of PKD2 by tyrosine phosphorylation, which in turn may have modulated the physiological functions of PKD2 during TCR-induced T cell activation.

A report of 21 unrecorded bacterial species of Korea belonging to the phylum Bacteroidota isolated in 2021

  • Chang-Jun Cha;Che Ok Jeon;Kiseong Joh;Wonyong Kim;Seung Bum Kim;Myung Kyum Kim;Jung-Hoon Yoon
    • Journal of Species Research
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    • v.12 no.spc2
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    • pp.23-32
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    • 2023
  • During screening for indigenous prokaryotic species in Republic of Korea in 2021, a total of 21 bacterial strains assigned to the phylum Bacteroidota were isolated from a variety of environmental habitats including pine cone, seaweed, soil, sea sediment, brackish water and moss. Based on the 16S rRNA gene sequence similarity value of more than 98.7% and formation of a robust phylogenetic clade with the type strain of the closest bacterial species, it was found that the 21 strains belong to independent and recognized bacterial species. There has been no official report that the identified 21 species have been isolated in Republic of Korea up to date. Therefore, 16 species in six genera of two families in the order Flavobacteriales, two species in two genera of two families in the order Cytophagales, one species in one genus of one family in the order Chitinophagales and two species in one genus of one family in the order Sphingobacteriales are proposed as unrecorded species of the phylum Bacteroidota isolated in Republic of Korea. Their Gram reaction, colony and cell morphology, basic phenotypic characteristics, isolation source, taxonomic status, strain ID and other information are described in the species descriptions.

Unilateral segmental odontomaxillary hypoplasia: an unusual case report

  • Pandey, Sushma;Pai, Keerthilatha M.;Nayak, Ajay G.;Vineetha, Ravindranath
    • Imaging Science in Dentistry
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    • v.41 no.1
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    • pp.39-42
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    • 2011
  • Facial asymmetry is not an uncommon occurrence in day to day dental practice. It can be caused by various etiologic factors ranging from facial trauma to serious hereditary conditions. Here, we report a rare case of non-syndromic facial asymmetry in a young female, who was born with this condition but was not aware of the progression of asymmetry. No relevant family history was recognized. She was also deficient in both deciduous and permanent teeth in the corresponding region of maxilla. Hence, the cause of this asymmetry was believed to be a segmental odontomaxillary hypoplasia of left maxilla accompanied by agenesis of left maxillary premolars and molars and disuse atrophy of corresponding facial musculature. This report briefly discussed the comparative features of segmental odontomaxillary hypoplasia, hemimaxillofacial dysplasia, and segmental odontomaxillary dysplasia and justified the differences between segmental odontomaxillary hypoplasia and the other two conditions.