نتایج جستجو برای: consanguinity marriage genetic counseling
تعداد نتایج: 659401 فیلتر نتایج به سال:
Sickle Cell Disease (SCD) is one of the most common severe autosomal recessively inherited blood disorders. In Saudi Arabia, the prevalence of this disease is significantly varied in different regions of the country, and the highest prevalence in the Eastern province of the country. A consanguineous marriage has been linked to the high incidence and prevalence of Sickle Cell Anemia (SCA), which...
This hospital based cross-sectional study describes the number of hemoglobinopathies in population southern Odisha during period and distribution each group hemoglobinopathy found according to their age, sex, clinical signs & symptoms, history consanguinity marriage parents, previous blood transfusion, siblings, socioeconomic status family, groups hematological parameters.
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Although a high proportion of marriages in Asia are consanguineous (i.e. contracted between close biological relatives), with some notable exceptions, there is a death of demographic and anthropological literature on the association between consanguinity and fertility. This paper presents an overview of the prevalence of consanguineous marriages in selected South and Southeast Asian countries, ...
Pastoral counselors who provide premarital counseling must address the topics that are most relevant to couples as they prepare for marriage. This article presents the results of a survey of clergy who provide premarital counseling, demonstrating the relative importance that clergy ascribe to premarital counseling topics, as well as the relationship between religious affiliation and ratings of ...
perrault's syndrome (p.s.) is rare. the combination of gonadal dysgenesis and hearing loss was accompanied by 46,xxkaryotype in three sisters with parental consanguineous marriage. genetic investigation revealed normal female karyotype, positive liarr and negative fluorescence ipj-bodies, which was confirmed by molecular study on the basis of fluorescence in situ hybridization (pish), with appl...
Background. Primary hyperoxaluria belongs to a group of rare metabolic disorders with autosomal recessive inheritance. It results from genetic mutations of the AGXT gene, which is more common due to higher consanguinity rates in the developing countries. Clinical features at presentation are heterogeneous even in children from the same family; this study was conducted to determine the clinical ...
The frequency of NIHF (Non-immunological hydrops fetalis) and congenital ascites associated with LSD (Lysosomal storage disorders) is exceptionally rare. The reported incidence worldwide is about 1% with very limited reports from the MENA (Middle East and North Africa) region despite high incidence of consanguinity in the area. We report a case of NIHF with subcutaneous edema and congenital asc...
The Birth abnormalities or congenital malformations can emerge during the fetal development stage from a parent's genetic composition. main contributors to neonatal and childhood disease impairment are abnormalities. Increase observation of anomaly (CA) in Mama Village that belong Kirkuk city has been made with information about frequency nature these This study was conducted estimate prevalenc...
Efficient computation of probabilistic relationships over family pedigrees is an important tool for a variety of problems in genetics, including genetic counseling and linkage analysis. The development of faster and more comprehensive algorithms has preoccupied geneticists for decades [?], and recent general-purpose algorithms for probabilistic inference over arbitrary networks (e.g., [?]) have...
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