• 제목/요약/키워드: Familial

검색결과 661건 처리시간 0.028초

도시 남성근로자의 생활시간구조분석 (Time-Use Analysis of Urban Employed Husbands)

  • Lee, Ki-Young;Song, Hye-Rim;Lee, Seung-Mi;Min, Sun-Seon;Seo, Ji-Won
    • 가정과삶의질연구
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    • 제14권1호
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    • pp.97-112
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    • 1996
  • This study is (1) to analyze urban employed husbands' time use applying a framework which classifies a day into public time familial time and individual time in order to demonstrate its disproportion in terms of their and their families' welfare(2) and to identify the related factors to their time use. Data for 280 husbands were gathered through structured questionnaire and time diary. Major findings are as follows; (1) Husband's time allocation is usually concentrated on their individual and public time while they spend relatively very short familial time. (2) Types of occupation age and wives' employment status are all related with husbands; time use but their sex-role attitude shows no significant relation.

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안구운동과 정신분열병 (Eye Movement and Schizophrenia)

  • 김철응
    • 수면정신생리
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    • 제3권1호
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    • pp.3-14
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    • 1996
  • Eye movement dysfunction has been found in large numbers of schizophrenia patients and their first-degree relatives and can be studied without the interference of deficits in attention, motivation, clinical status and medication effects with relatively easy method. Eye movement dysfunction has been proposed as a useful way of expanding the schizophrenia phenotype in genetic studies. I review the literature on eye movement dysfunction with respect to syndrome and familial specificity and the quantitative assessment of eye tracking. I hope that the etiology and the pathophysiology of schizophrenia can be clarified through this eye movement study.

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가계내 재산상속 행동에 관한 탐색적 연구 - Ethnographic 접근 방식을 중심으로- (An Exploratory Study of Household Inheritance Based on Ethnographic Approach)

  • 박명희;정주원
    • 대한가정학회지
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    • 제38권2호
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    • pp.91-107
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    • 2000
  • The purpose of this study is to understand the familial and economic problems(household-financial management) came out as a result of inheritance in household with a qualitative Ethnographic interview analysis method. As a result of interview, we found out three results; first, inheritance consciousness, attitude of predecessor(parents generation) second, the changes in familial economic relationship by inheritance stages (pre-inheritance stage, inheritance progressing stage, post-inheritance stage) third, the emotional changes of predecessor(paraents generation). The results indicated that there were significant importance and influence of household inheritance, therefore, the necessities of definite and systemic old-aged plan with financial management of inheritance should be introduced.

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자매의 두개악안면골에 발생된 다골섬유성이형성증의 증례보고 (2CASE REPORTS OF THE POLYOSTOTIC FIBROUS DYSPLASIA ON THE CRANIAL AND MAXILLO FACIAL BONES OF THE SISTERS)

  • 김한평;박창서
    • 치과방사선
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    • 제9권1호
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    • pp.37-43
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    • 1979
  • The authors observed 2 cases of fibrous dysplasia on the cranial and maxillofacial bones in 31, 28 aged sisters, who had come to the Infirmary of Dental College, Yonsei University. The serial roentgenograms and clinical findings had been taken and the results established as polyostotic fibrous dysplasia according to the findings in their images. The authors have obtained the results as follows: 1. Bony expansion of the mandible occured at 18 years of age and the facial assymetry appeared due to development of the lesions. 2. The traumatic history were not noted but weak tendency of familial history noted 3. Endocrine disturbances, hyperpigmentation on the skin and premature puberty in the infancy were not noted. 4. We have concluded these diseases as polyostotic fibrous dysplasia on the cranial and maxillofacial bones with weak familial tendency according to the findings

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Experiences of Overcoming Alcoholism in Alcoholics' Female Spouses Using Al-Anon

  • Sim, Jeong Eun;Hwang, Seon Young
    • 지역사회간호학회지
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    • 제29권2호
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    • pp.194-205
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    • 2018
  • Purpose: The aim of this study is to investigate and elucidate actual experiences of alcoholics' spouses using familial social gatherings. Methods: A total of nine women whose alcoholic husbands were attending Al-Anon meetings held in Y Cathedral in S District of Seoul were included in this study. Data collection of this study was conducted through in-depth interviews with participants from September 24 to November 30, 2015. Data analysis was conducted at the same time as the data collection, and analysis was performed according to the method suggested by Colaizzi(1978). Results: We categorized the participants' experiences into five themes including 'Trapped in a Deep Dark Tunnel', 'Life of Walking in an Endless Tunnel', 'Reaching a Dead End', 'Walking towards a Ray of Light', 'Finding Oneself on a Strange Path'. Conclusion: The results of this study provide an understanding of the essential structure of the life experiences of alcoholic spouses using familial social gatherings.

브로카실어증으로 발현한 가족성 V180I 변이 Creutzfeldt-Jakob병 (Familial Creutzfeldt-Jakob Disease with V180I Mutation Presented with Broca's Aphasia)

  • 김정연;이덕수;박경원
    • 대한신경과학회지
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    • 제36권4호
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    • pp.345-349
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    • 2018
  • Familial Creutzfeldt-Jakob Disease (fCJD) is characteristic with older age onset, relatively low occurrence rate, slower progression and lower possibility of developing myoclonus, cerebellar, pyramidal signs and visual disturbance compared with classical sporadic CJD. We report a case of 75-year-old male patient presented with sudden onset of right side weakness with Broca's aphasia who has been diagnosed with fCJD with V180I mutation. This case indicates that fCJD with V180I mutation can have stroke-like initial presentation.

Cohen-Gibson syndrome in a family: The first familial case report

  • Kang, Yeo Jin;Kim, Young Ok
    • Journal of Genetic Medicine
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    • 제18권1호
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    • pp.70-74
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    • 2021
  • Cohen-Gibson syndrome (CGS) was first reported by Cohen et al., who identified the mutation of the gene encoding the embryonic ectoderm development (EED) in a patient with phenotypes similar to Weaver syndrome. CGS manifests as an overgrowth and intellectual disability, in addition to the characteristic facial features and organ anomalies. CGS has been reported in only 11 unrelated patients since 2015. A girl aged 6 years and 3 months presented with seizures. She had macrosomia, a dysmorphic face, and intellectual disability. Her mother and younger sister and brother also had macrosomia, intellectual disability, and similar facial features; additionally, her mother experienced seizures and had an arachnoid cyst, while her siblings had valvar pulmonary stenosis. Whole-exome sequencing for the proband revealed a mutation of EED (c.581A>G, p.Asn194Ser), which was also verified in the mother and both siblings using Sanger sequencing. This is the first report of familial CGS.

보편 서사로서의 가족희극, 인스 최의 『김씨네 편의점』 (Universal Narrative of a Familial Comedy: Ins Choi's Kim's Convenience)

  • 이용희
    • 미국학
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    • 제44권2호
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    • pp.67-96
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    • 2021
  • The Canadian public broadcaster CBC had successfully aired a sitcom centered on a Korean immigrant family from 2016 to 2021. The show is based on the play Kim's Convenience written by a Korean-Canadian playwright Ins Choi. This study explores literary features of Kim's Convenience that accounts for its popularity; three elements of the show play crucial roles in maintaining the balance between specificity and universality. First, Choi deploys a Korean immigrant story in the form of comedy. Second, the main plot revolves around an ordinary family with generational strains that ends in reconciliation. Third. the Kims are depicted more as an archetypical family than a stereotypically Asian one. By closely interweaving these elements, Choi induces the audience to find commonalities from the show, and racial specificities of the Kim's family become "spicy" attractions of the play.

Successful Use of Bortezomib for Recurrent Progressive Familial Intrahepatic Cholestasis Type II After Liver Transplantation: A Pediatric Case with a 9-Year Follow-Up

  • Yu Gyoung Bak;Ho Jung Choi;Yeong Eun Kim;Seak Hee Oh;Kyung Mo Kim
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제27권1호
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    • pp.71-76
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    • 2024
  • Recurrence of progressive familial intrahepatic cholestasis (PFIC) type II poses challenges during postoperative liver transplant care. Posttransplant patients with PFIC type II risk developing recurrent cholestasis with normal gamma-glutamyl transferase activity, which mimics the original bile salt export pump (BSEP) protein deficiency and is related to a form of immunoglobulin G antibody (anti-BSEP)-mediated rejection. Bortezomib effectively induces apoptosis of actively antibody-producing plasma cells that may have a role in antibodymediated rejection. In this case, we used bortezomib to treat PFIC type II recurrence after liver transplantation in a child.