We evaluate the association of familial factors and suicidality among transgender adults in U.S. by estimating odds lifetime suicide ideation attempt using 2015 Transgender Survey. Predictors include family support, rejection, specific experiences related to both. About 79% sample respondents have experienced suicidal nearly 43% made a attempt. The predicted probability is 0.35 for those with n...

background and purpose: identifying the risk factors of hepatitis c، b، and hiv is necessary to prevent their increasing prevalence. therefore، we sought to identify the frequency of their risk factors among the homeless of tehran، iran during 2005 to 2007. methods and materials: this descriptive analytical study was conducted during 2005 to 2007 on the homeless population of tehran، iran. two ...

amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disorder of the motor neurons in the spinal cord, brainstem, and motor cortex. ten percent of als cases are familial with both autosomal dominant and recessive modes of inheritance. mutations in the copper/zinc superoxidedismutase-1 (sod-1) gene, the first gene linked with als, result in sod-1 gene accounting for ~ 20% of fa...

Abstract Singles—here understood as unmarried or never married individuals—are a growing subset of the Japanese population that has not received discrete attention in context COVID-19 pandemic. This article addresses ways which pandemic and its associated interventions—calls for social distancing, self-restraint, avoidance ‘3Cs’—affect singles’ (non)familial personal relationships practices int...

Limiting the success of breast cancer surgery in Bulgaria, sometimes diagnosis is very late. Genetic markers for breast cancer are not well known to the surgeons and they are not available for practical use. Appropriate psychological support is not available in every case, because the psychologists are not well informed about clinical and genetic aspects of the illness. There have been limited ...

aplasia cutis conginita (acc) is a condition characterized by congenital absence of skin, usually on the scalp. acc can occur as an isolated condition or in the presence of other congenital anomalies. here we describe a case of a 16 days old baby girl with an isolated acc of the scalp. her elder two siblings have been diagnosed with acc with concomitant cardiac or limb anomalies. the patient wa...

background: it is presumed that gastric cancer has several etiologies. first-degree relatives of patients with gastric cancer are suggested to be at higher risk compared to others. this is the first study aimed at estimating this risk, using meta-analysis of case-control studies. materials and methods: all records prior to february 2008 in pubmed and embase were searched for case-control studie...

objective(s):familial mediterranean fever (fmf), an inherited autosomal recessive disorder, is frequently present among individuals of mediterranean origin. differences in the clinical manifestations of fmf between different ethnic groups have been documented. the aim of the present study was to determine the most common characteristics of fmf and the relationship between clinical findings and ...

in general, both common illnesses and rare diseases can develop in people and their relatives in families. therefore, taking family history is an effective screening tool to detect such diseases and patients should be aware of its importance in families’ health with updating information in regular visiting. for more information on identifying the genetic pattern of diseases, in this article, we...

background: familial mediterranean fever (fmf) is an autosomal recessive genetic disorder characterized by recurrent episodes of self-limited fever and serosal tissues inflammation. methods: to evaluate clinical symptoms and common genetic mutations in southwestern iranian patients with fmf, 20 unrelated patients were enrolled in this study based on clinical criteria. a panel of 12 common mefv ...