نتایج جستجو برای: familial history

تعداد نتایج: 402168  

Journal: :Turk pediatri arsivi 2014
Bahar Büyükkaragöz Mesut Koçak Emine Hafize Erdeniz Aysun Çaltık Yılmaz Uğur Ufuk Işın Zennure Takcı Servet Güreşci Sacit Günbey

An eight-year old boy who was healthy previously had a history of use of trimethoprime-sulphametoxsazole (TPM-SMX) because of diarrhea ten days before presentation. He was hospitalized because painful swelling occured in the legs under this treatment, he had fever and joint pain for the last five days. In his personal history, there was no pathology except for frequent aphtous ulcers in the mou...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2002
Kari Hemminki Kamila Czene

Population attributable faction (PAF) shows the proportion of the disease that could be prevented if the cause could be removed. PAFs for most types of familial cancer have not been determined. We used the Swedish Family-Cancer Database on 10.2 million individuals and 688,537 parental and 116,741 offspring cancers to calculate familial risks, proportions of affected individuals, and familial PA...

2011
Man-huei Chang Rodolfo Valdez Renée M. Ned Tiebin Liu Quanhe Yang Ajay Yesupriya Nicole F. Dowling James B. Meigs Michael S. Bowen Muin J. Khoury

OBJECTIVE To test the association of family history of diabetes with the adoption of diabetes risk-reducing behaviors and whether this association is strengthened by physician advice or commonly known factors associated with diabetes risk. RESEARCH DESIGN AND METHODS We used cross-sectional data from the 2005-2008 National Health and Nutrition Examination Survey (NHANES) to examine the effect...

Journal: :Archives of general psychiatry 1998
K R Merikangas M Stolar D E Stevens J Goulet M A Preisig B Fenton H Zhang S S O'Malley B J Rounsaville

BACKGROUND There is increasing evidence that substance use disorders are familial and that genetic factors explain a substantial degree of their familial aggregation. To perform a controlled family study of probands with several different predominant drugs of abuse, including opioids, cocaine, cannabis, and/or alcohol. METHODS The subjects for the present study included 231 probands with depe...

Journal: :The Lancet. Neurology 2013
Martin R Turner Orla Hardiman Michael Benatar Benjamin R Brooks Adriano Chio Mamede de Carvalho Paul G Ince Cindy Lin Robert G Miller Hiroshi Mitsumoto Garth Nicholson John Ravits Pamela J Shaw Michael Swash Kevin Talbot Bryan J Traynor Leonard H Van den Berg Jan H Veldink Steve Vucic Matthew C Kiernan

Two decades after the discovery that 20% of familial amyotrophic lateral sclerosis (ALS) cases were linked to mutations in the superoxide dismutase-1 (SOD1) gene, a substantial proportion of the remainder of cases of familial ALS have now been traced to an expansion of the intronic hexanucleotide repeat sequence in C9orf72. This breakthrough provides an opportunity to re-evaluate longstanding c...

Journal: :Journal of Medical Case Reports 2008
Jason Robin Sheridan Meyers Maher Nahlawi Jyothy Puthumana Jon Lomasney David Mehlman Vera Rigolin Charles Davidson

INTRODUCTION Hereditary amyloidodis is a rare disease process with a propensity to cause polyneuropathies, autonomic dysfunction, and restrictive cardiomyopathy. It is transmitted in an autosomal dominant manner, with disease onset usually in the 20s-40s. The most common hereditary amyloidogenic protein, transthyretin, is synthesized in the liver and lies on Chromosome 18. Over 80 amyloidogenic...

Journal: :The Laryngoscope 2015
Jeon Mi Lee Mi Joo Kim Jinsei Jung Hyun Ji Kim Young Joon Seo Sung Huhn Kim

OBJECTIVES/HYPOTHESIS This study was undertaken to investigate the prevalence, inheritance patterns, and clinical characteristics of familial Meniere's disease (MD) in a South Korean population. STUDY DESIGN Direct interviews, telephone interviews, and reviews of the medical records of definite Meniere's disease patients and their families. METHODS Direct and telephone interviews were perfo...

Journal: :Endocrine-related cancer 2013
Raquel G Martins Joana B Nunes Valdemar Máximo Paula Soares Joana Peixoto Telmo Catarino Teresa Rito Pedro Soares Luísa Pereira Manuel Sobrinho-Simões Ana Paula Santos Joana Couto Rui Henrique Joana Matos-Loureiro Paula Dias Isabel Torres Jorge Lima

We would like to report a genetic screening of SDHB, SDHC, SDHD and SDHAF2 genes (hereafter abbreviated to SDHx) in patients with paragangliomas (PGL) and phaeochromocytomas (PCC) from northern Portugal. PGL and PCC are neuroendocrine tumours that can be caused by heterozygous germline loss-of-function mutations in SDHx genes (Gimenez-Roqueplo et al. 2012). The spectrum of germline SDHx mutatio...

Journal: :Psychological medicine 1998
D L Foley M C Neale K S Kendler

BACKGROUND In unselected samples, the diagnosis of major depression (MD) is not highly reliable. It is not known if occasion-specific influences on reliability index familial risk factors for MD, or how reliability is associated with risk for co-morbid anxiety disorders. METHODS An unselected sample of 847 female twin pairs was interviewed twice, 5 years apart, about their lifetime history (L...

2017
Akshita Gupta Sawan Bopanna Saurabh Kedia Dawesh Prakash Yadav Sandeep Goyal Saransh Jain Govind Makharia Vineet Ahuja

BACKGROUND/AIMS Familial occurrence of inflammatory bowel disease (IBD) is well documented. Reports from Western countries have shown a higher familial occurrence of ulcerative colitis (UC) in first- and second-degree relatives than that in the Asian UC population. No data are currently available from the Indian subcontinent in this regard. We present our data on the familial aggregation of UC....

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