...women (25.9%). Most of those infected had a high pH of vaginal secretion. O’Brien et al. (2010) state that infertility affects approximately 15% of couples and genetic abnormalities account for 15-30% of infertility in men. Genetics plays a role by affecting the hormonal level, sperm quality and spermatogenesis. The article mentions several genetic abnormalities with phenotype to show the prevalence in men. O’Brien et al. state that aneuploidy (incorrect chromosome number) is the most common cause of chromosome abnormality in infertile men. Chromosomal abnormalities with phenotype Azoospermia to normozoospermia had a prevalence rate of 5% in total infertile population and 15% in Azoospermic population. Kleinfelters syndrome, genetic disorder in which one has an extra x chromosome, with phenotype Azoospermia to severe oligozoospermia had a prevalence rate of 5% severe oligozoospermia and 10% Azoospermia in male infertility. ...
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...Infertility is estimated to affect as many as 186 million people worldwide. Although male infertility contributes to more than half of all cases of global childlessness, infertility remains a woman’s social burden. Marcia C. Inhorn, and Pasquale Patrizio (2015). Infertility around the globe: new thinking on gender, reproductive technologies and global movements in the 21st century. Human Reproduction Update, Vol.21, No.4 pp. 411–426, 2015 However, infertility should be regarded as a two-patient disorder, including both partners. So a work-up for both male and female partners must be thoroughly evaluated, counseled, and included in the therapeutic decision-making processes. The cornerstone for diagnosis starts with a detailed history taking,...
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...Statistically, one-third of infertility problems are related to men and the remaining one-third is a combination of fertility factors involving both partners or unknown causes. “The most common causes of male infertility are azoospermia (no sperm cells are produced) and oligospermia (only a few sperm cells are produced)” (American Pregnancy Association). Sometimes, infertility is caused by the sperms cells malforming or dying before they reach the egg. Infertility in men is, rarely, caused by genetic diseases like cystic fibrosis. The most common cause of female infertility is ovulation disorders. “Ovulation disorders occur when ovulation is disrupted or absent” (Create Fertility). Other causes of infertility in women can be a result of blocked fallopian tubes, birth defects of the uterus, uterine fibroids, and...
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...Introduction The new reproductive technology (NRT) is no exception any more, since Louise Brown, the first "test tube" baby, was born on 25 July, 1978 (Simmons, 2009). Before her parents Lesley Brown and John Brown met Drs Edwards and Steptoe, they had been trying to conceive a baby for nine years, but never succeeded. Because Lesley Brown was diagnosed with fallopian tubes obstruction, at that time, it indeed meant hopelessness of being pregnant without a miracle. Then the ungovernable longings for having a baby impelled Lesley Brown to participated in Drs Edwards and Steptoe's experiments. Lesley Brown was not the only volunteer during the procedure, but she fortunately became the first successful case (Deech & Smajdor,2007). At present, 4 million "test tube" babies have been born around the world(website), thanks to Drs Edwards and Steptoe's great contribution from 1977. But what if geneticists announce that genetics and traits can be predetermined for unborn babies today? Then what will parents order for their new babies? Blond hair or ruddy eyes? Bird’s wings or fish's gills? How about the mermaid’s beauty and Einstein's intelligence? Those questions need to be reflected by young generations, because that may be no longer an imagination of the future. Jeffrey Steinberg, a pioneer of in vitro fertilization (IVF), and the founder of the LA Fertility Institute as well, has already maintained in 2009 that his clinic would carry out trait-selected serves soon (Mara,...
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...One important detail that teenagers fail to realize is that taking steroids at this phase in their development can and will have long term ramifications. This type of androgenic steroid can cause the early closure of physes in children and adolescents preventing them from achieving their full height due to an interruption of natural development (Fitness, 1997). Examples of short term effects anyone abusing this type of steroid may have are hair loss, increased aggression, depression, or suicidal tendencies, high blood pressure, alterations in cholesterol or blood lipids and increased rate of muscle strains. Boys may experience gynecomastia, shrinking of testicles, and azoospermia. While young women may begin having menstrual irregularities, excessive facial or body hair growth, infertility, clitoromegaly, and a deeper voice that may remain even when the steroids are no longer taken (Anabolic, n.d.). Long term effects that can manifest years after abuse are liver, heart, and kidney diseases depending on what type of anabolic steroid was abused and how the body metabolizes it. Other factors that are not always considered is that the steroids affect a part of the brain called the limbic system that controls mood. “Long-term steroid abuse can lead to aggressive behavior and extreme mood swings. This is...
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...chloride transport activity (Wainwright 2015). Class III mutations are mutations that are found in the nucleotide binding domains (Vankeergerghen 2002). They also interfere with the binding of ATP to the binding domains, as well as the stimulation of the channel by ATP which results in a decrease of net chloride transport activity (Vankeergerghen 2002). Class IV mutations cause a defective CFTR channel by affecting the amino acids located in the pores of the channel (Vankeergerghen 2002). This leads to a defective channel with conduction problems (Vankeergerghen 2002). Class V mutations are mutations that can be found in the CFTR gene that not only result in CF, but can also cause congenital bilateral absence of the vas deferens, obstructive azoospermia, disseminated bronchiectasis, allergic bronchopulmonary aspergillosis, hypertyrosinemia, and chronic pancreatitis (Vankeergerghen 2002). Due to the fact that the vase deferens become blocked later in life in CF-males, 97% of them are infertile (Vankeergerghen 2002). Mutations like these cause a decrease in CFTR protein production (Vankeergerghen 2002). Class VI mutations affect not only the chloride channel, but other ion channels specifically the regulatory properties of these channels. (Vankeergerghen 2002) One of the biggest issues in trying to find a cure for Cystic Fibrosis is finding a model organism that can replicate the phenotypes of the disease (Stoltz 2015). The issue with mice is they are able to have the CFTR mutations,...
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...[pic] Term paper Stem cell therapy Irfan manzoor. Roll no: RP7002B22. Reg. no: 11000225. Course: Bsc. Biotech 1. Lovely professional university Contents 1. Stem cells and properties. 2-3 2. Stem cell therapy. 5-12 3. Stem cell use in animals 13-15 4. Recent researches in stem cell therapy 16-19 5. Conclusion 21 6. Bibliography 22 Stem cells Stem cells are cells found in all multi cellular organisms. They are characterized by the ability to renew themselves through mitotic cell division and differentiate into a diverse range of specialized cell types. Research in the stem cell field grew out of findings by Ernest A. McCulloch and James E. Till at the University of Toronto in the 1960s. The two broad types of mammalian stem cells are: embryonic stem cells that are isolated from the inner cell mass of blastocysts, and adult stem cells that are found in adult...
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