This paper aims to provide an interdisciplinary approach fertility analysis. The main objective is the use of a psychotherapeutic tool in decision We used genogram, frequently utilized systemic psychotherapy. By borrowing and using genogram context analysis, it facilitates our understanding terms individual family factors, as well cultural, economic social factors. article study process resulti...

Abstract Background Molecular genetic diagnostics (GDx) is an increasingly used tool in the so-called ‘precision medicine'. For a structured implementation of GDx screening programmes (SP), organisational and ethical implications must be considered. Our research report addresses aspects different health care systems considerations context familial hypercholesterolaemia (FH)-a malfunction lipid ...

familial colloid cyst of the third ventricle is very rare. this is one of the two largest families reported and the first in which all affected members are siblings. one asymptomatic sister was found by screening, emphasizing the value of screening. a brother and two sisters from a family consisting of three brothers and three sisters who were diagnosed as having colloid cyst of the third ventr...

<p>With governance increasingly regarded as co-governance, states’ capacity to steer, correct, and discipline a wide range of self-governing actors becomes crucial for effectiveness, efficiency, democracy. This article investigates that the relationship between formal institutions customary self-governance in areas limited statehood. In South Sudan, field land can be an area As relations ...

Background: Familial chylomicronemia syndrome is a rare disorder of lipoprotein metabolism due to familial lipoprotein lipase or apolipoprotein C-II deficiency or the presence of inhibitors to lipoprotein lipase. It manifests as eruptive xanthomas, acute pancreatitis, and lipaemic plasma due to marked elevation of triglyceride and chylomicrons levels. Case presentation: We report a rare case of...

abstract bachground and aim: mutation analysis of mitochondrial genome and brca genes are helpful in the early diagnosis of familial breast cancers. in this study, we investigated mitochondrial common deletion and brca mutations through multiplex pcr and clinical parameters for the detection of familial breast cancers in archival breast cancer samples. methods: the multiplex pcr was conducted o...

background: in northeastern iran there is an area of high incidence of esophageal cancer which is populated by residents of turkmen ancestry. several environmental risk factors for esophageal cancer have been proposed, but the roles of familial and genetic factors have not been studied extensively in the turkmen population. materials and methods: we evaluated the importance of familial risk fac...

introduction: due to the whole network of polyposis registers worldwide and early prophylactic treatment, survival of familial adenomatosis (fap) patients is improved. extracolonic manifestations are remarkable feature of fap. two extracolonic manifestations (duodenal adenomatosis, leading duodenal cancer and desmoid tumours) play a very important role in the reasons of death in polyposis popul...