Also during all this I was working on the shelves some more and added some embellishments to them. So here are the pics.
Tuesday, September 22, 2009
Completing the name on the wall
So I have been working on the name on the wall for Miabelle. And I finally finished. I bought the letters, bought the paint....grabbed all the little things and went to town.
Also during all this I was working on the shelves some more and added some embellishments to them. So here are the pics.
Also during all this I was working on the shelves some more and added some embellishments to them. So here are the pics.
Wednesday, September 16, 2009
Another contest ....... Sounds good!!
The Cloth Diaper Experiment is having a contest for a baby food processor. I entered and I think everyone should if they have little ones. Go check it out:
beaba babycook review and giveaway
beaba babycook review and giveaway
Awake to good news :)
So this morning I get up and check my mail to find the best thing ever.
Fuzzi Bunz One Size Giveaway winner is ME!!!!
Which means I get 3 of these diapers. I have never won anything. Atleast not without working my butt off and then it was only a necklace.
But it is not just about the win. I learn more from Kari and her blog than I do from searching the internet sometimes. She is a lovely mom and a good internet company.
Again thanks Kari!!
And I can not wait to see the new diapers :)
Fuzzi Bunz One Size Giveaway winner is ME!!!!
Which means I get 3 of these diapers. I have never won anything. Atleast not without working my butt off and then it was only a necklace.
But it is not just about the win. I learn more from Kari and her blog than I do from searching the internet sometimes. She is a lovely mom and a good internet company.
Again thanks Kari!!
And I can not wait to see the new diapers :)
Thursday, September 10, 2009
Cloth Diaper Inserts
So I have been making cloth diaper inserts lately. I took alot of old fleece, wool, microfleece and whatever I found that might absorb good and making inserts out of them. Not only is it cost effective but it removes my old stash so I can buy new stash. So here is what i have so far both made and unmade. I am working hard and getting these completed and sent to friends who are cloth diapering too. Maybe I will eventually do it to make money.
Wednesday, September 2, 2009
Factor V Lieden- Wikipedia
Factor V Leiden (sometimes Factor VLeiden) is the name given to a variant of human factor V that causes a hypercoagulability disorder. In this disorder the Leiden variant of factor V cannot be inactivated by activated protein C.[1] Factor V Leiden is the most common hereditary hypercoagulability disorder amongst Eurasians.[2][3][4] It is named after the city Leiden (The Netherlands), where it was first identified in 1994 by Prof R. Bertina et al.[5]
Factor V Leiden is an autosomal dominant condition which exhibits incomplete dominance and results in a Factor V variant which cannot be as easily degraded by aPC. The gene that codes the protein is referred to as F5. Mutation of this gene—a single nucleotide polymorphism (SNP) is located in exon 10.[6] As a missense substitution it changes a protein's amino acid from arginine to glutamine. Depending on the chosen start the position of the nucleotide variant is either at position 1691 or 1746.[7] It also affects the amino acid position for the variant which is either 506 or 534. Together with the general lack of nomenclature standard it means that the SNP can be referred to in several ways such as G1691A, c.1601G>A, 1691G>A, c.1746G>A, p.Arg534Gln, Arg506Gln, R506Q or rs6025! Since this amino acid is normally the cleavage site for aPC, the mutation prevents efficient inactivation of factor V. When factor V remains active, it facilitates overproduction of thrombin leading to excess fibrin generation and excess clotting.
The excessive clotting that occurs in this disorder is almost always restricted to the veins, where the clotting may cause a deep vein thrombosis (DVT). If the venous clots break off, these clots can travel through the heart to the lung, where they block a pulmonary blood vessel and cause a pulmonary embolism. Women with the disorder have an increased risk of miscarriage and stillbirth. It is extremely rare for this disorder to cause the formation of clots in arteries that can lead to stroke or heart attack, though a "mini-stroke", known as a transient ischemic attack, is more common . Given that this disease displays incomplete dominance, those who are homozygous for the mutated allele are at a heightened risk for the events detailed above versus those that are heterozygous for the mutation.
Up to 30% of patients who present with deep vein thrombosis (DVT) or pulmonary embolism have this condition. Factor V Leiden doubles the risk that a person will have a DVT during their life, but it is unclear whether these individuals are at increased risk for recurrent venous thrombosis. While only 1% of people with factor V Leiden have two copies of the defective gene, these homozygous individuals have a more severe clinical condition. The presence of acquired risk factors for venous thrombosis—including smoking, use of estrogen-containing (combined) forms of hormonal contraception use, and recent surgery—further increase the chance that an individual with the factor V Leiden mutation will develop DVT.
Women with Factor V Leiden have a substantially increased risk of clotting in pregnancy (and on estrogen-containing birth control pills or hormone replacement) in the form of deep vein thrombosis and pulmonary embolism. They also may have a small increased risk of preeclampsia, may have a small increased risk of low birth weight babies, may have a small increased risk of miscarriage and stillbirth due to either clotting in the placenta, umbilical cord, or the fetus (fetal clotting may depend on whether the baby has inherited the gene) or influences the clotting system may have on placental development.[8] Note that many of these women go through one or more pregnancies with no difficulties, while others may repeatedly have pregnancy complications, and still others may develop clots within weeks of becoming pregnant.
There are a few different methods by which this disease can be diagnosed. Most laboratories screen 'at risk' patients with either a snake venom (e.g. dilute Russell's viper venom time) based test or an aPTT based test. In both methods, the time it takes for blood to clot is shortened in the presence of the factor V Leiden mutation. This is done by running two tests simultaneously, one test is run in the presence of activated protein C (APC) and the other, in the absence. A ratio is determined based on the two tests and the results signify to the laboratory whether APC is working or not. These are quick, three minute, automated tests that most hospital laboratories can easily perform.
There is also a genetic test that can be done for this disorder. The mutation (a 1691G→A substitution) removes a cleavage site of the restriction endonuclease MnlI, so PCR, treatment with MnlI, and then DNA electrophoresis will give a diagnosis.
Content |
Pathophysiology
In the normal person, factor V functions as a cofactor to allow factor X to activate an enzyme called thrombin. Thrombin in turn cleaves fibrinogen to fibrin, which polymerizes to form the dense meshwork that makes up the majority of a clot. Activated protein C (aPC) is a natural anticoagulant that acts to limit the extent of clotting by cleaving and degrading factor V.| SNP: Factor V Leiden | ||
|---|---|---|
| Name(s) | Factor V Leiden, Arg506Gln, R506Q, G1691A | |
| Gene | F5 | |
| Chromosome | 1 | |
| External databases | ||
| Ensembl | Human SNPView | |
| dbSNP | 6025 | |
| HapMap | 6025 | |
| SNPedia | 6025 | |
| HgenetInfoDB | 6025 | |
| ALFRED | SI001216K | |
The excessive clotting that occurs in this disorder is almost always restricted to the veins, where the clotting may cause a deep vein thrombosis (DVT). If the venous clots break off, these clots can travel through the heart to the lung, where they block a pulmonary blood vessel and cause a pulmonary embolism. Women with the disorder have an increased risk of miscarriage and stillbirth. It is extremely rare for this disorder to cause the formation of clots in arteries that can lead to stroke or heart attack, though a "mini-stroke", known as a transient ischemic attack, is more common . Given that this disease displays incomplete dominance, those who are homozygous for the mutated allele are at a heightened risk for the events detailed above versus those that are heterozygous for the mutation.
Epidemiology
Studies have found that about 5% of Caucasians in North America have factor V Leiden. The disease is less common in Hispanics and African-Americans and is extremely rare in people of Asian descent.Up to 30% of patients who present with deep vein thrombosis (DVT) or pulmonary embolism have this condition. Factor V Leiden doubles the risk that a person will have a DVT during their life, but it is unclear whether these individuals are at increased risk for recurrent venous thrombosis. While only 1% of people with factor V Leiden have two copies of the defective gene, these homozygous individuals have a more severe clinical condition. The presence of acquired risk factors for venous thrombosis—including smoking, use of estrogen-containing (combined) forms of hormonal contraception use, and recent surgery—further increase the chance that an individual with the factor V Leiden mutation will develop DVT.
Women with Factor V Leiden have a substantially increased risk of clotting in pregnancy (and on estrogen-containing birth control pills or hormone replacement) in the form of deep vein thrombosis and pulmonary embolism. They also may have a small increased risk of preeclampsia, may have a small increased risk of low birth weight babies, may have a small increased risk of miscarriage and stillbirth due to either clotting in the placenta, umbilical cord, or the fetus (fetal clotting may depend on whether the baby has inherited the gene) or influences the clotting system may have on placental development.[8] Note that many of these women go through one or more pregnancies with no difficulties, while others may repeatedly have pregnancy complications, and still others may develop clots within weeks of becoming pregnant.
Diagnosis
Suspicion of factor V Leiden being the cause for any thrombotic event should be considered in any white patient below the age of 45, or in any person with a family history of venous thrombosis.There are a few different methods by which this disease can be diagnosed. Most laboratories screen 'at risk' patients with either a snake venom (e.g. dilute Russell's viper venom time) based test or an aPTT based test. In both methods, the time it takes for blood to clot is shortened in the presence of the factor V Leiden mutation. This is done by running two tests simultaneously, one test is run in the presence of activated protein C (APC) and the other, in the absence. A ratio is determined based on the two tests and the results signify to the laboratory whether APC is working or not. These are quick, three minute, automated tests that most hospital laboratories can easily perform.
There is also a genetic test that can be done for this disorder. The mutation (a 1691G→A substitution) removes a cleavage site of the restriction endonuclease MnlI, so PCR, treatment with MnlI, and then DNA electrophoresis will give a diagnosis.
References
- Comparison of Russell viper venom-based and activated partial thromboplastin time-based screening assays for resistance to activated protein C. Am J Clin Pathol. 2008 Nov;130(5):796-804. Herskovits AZ, Lemire SJ, Longtine J, Dorfman DM. Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.[1][dead link]
- Press, R. D., Bauer, K. A., Kujovich, J. L., Heit, J. A. (2002) Arch Pathol Lab Med 126, 1304-1318. "Clinical Utility of Factor V Leiden (R506Q) Testing for the Diagnosis and Management of Thromboembolic Disorders"
- ^ De Stefano V, Leone G (1995). "Resistance to activated protein C due to mutated factor V as a novel cause of inherited thrombophilia". Haematologica 80 (4): 344–56. PMID 7590506. http://www.haematologica.org/cgi/content/abstract/80/4/344.
- ^ Ridker PM, Miletich JP, Hennekens CH, Buring JE (1997). "Ethnic distribution of factor V Leiden in 4047 men and women. Implications for venous thromboembolism screening". JAMA 277 (16): 1305–7. doi:10.1001/jama.277.16.1305. PMID 9109469.
- ^ Gregg JP, Yamane AJ, Grody WW (December 1997). "Prevalence of the factor V-Leiden mutation in four distinct American ethnic populations". Am. J. Med. Genet. 73 (3): 334–6. doi:10.1002/(SICI)1096-8628(19971219)73:3<334::AID-AJMG20>3.0.CO;2-J. PMID 9415695.
- ^ De Stefano V, Chiusolo P, Paciaroni K, Leone G (1998). "Epidemiology of factor V Leiden: clinical implications". Semin. Thromb. Hemost. 24 (4): 367–79. doi:10.1055/s-2007-996025. PMID 9763354.
- ^ Bertina RM, Koeleman BP, Koster T, et al. (1994). "Mutation in blood coagulation factor V associated with resistance to activated protein C". Nature 369 (6475): 64–7. doi:10.1038/369064a0. PMID 8164741.
- ^ "SNP linked to Gene F5". NCBI. http://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?locusId=2153.
- ^ Jennifer Bushwitz, Michael A. Pacanowski, and Julie A. Johnson (2006-10-11). "Important Variant Information for F5". PharmGKB. http://www.pharmgkb.org/search/annotatedGene/f5/variant.jsp.
- ^ Rodger MA et al.Inherited Thrombophilia and Pregnancy Complications Revisited.Obstet Gynecol. 2008 Aug;112(2 Pt 1):320-4.
Further reading
- Hooper WC, De Staercke C (2006). "The relationship between FV Leiden and pulmonary embolism". Respir. Res. 3: 8. doi:10.1186/rr180. PMID 11806843.
- Nicolaes GA, Dahlback B (2002). "Factor V: Factor V and thrombotic disease: description of a janus-faced protein". ATVB 22 (4): 530–538. PMID 11950687.
- Andreassi MG, Botto N, Maffei S (2006). "Factor V Leiden, prothrombin G20210A substitution and hormone therapy: indications for molecular screening". Clin. Chem. Lab. Med. 44 (5): 514–21. doi:10.1515/CCLM.2006.103. PMID 16681418.
- Segers K, Dahlback B, Nicolaes GA (2007). "Coagulation factor V and thrombophilia: background and mechanisms.". Thrombosis Haemost. 98 (3): 530–542. PMID 17849041.
External links
- MeSH factor+V+Leiden
- Kujovich JL, Goodnight SH (2007-02-17). "Factor V Leiden Thrombophilia". GeneReviews. University of Washington, Seattle. http://www.genetests.org/profiles/factor-v-leiden/index.html. Retrieved 2008-06-20.
- Smith DO (2008-05-12). "Thrombophilia Awareness Project". http://www.fvleiden.org/. Retrieved 2008-06-20. "Information for those living with thrombophilia"
- National Alliance for Thrombosis and Thrombophilia - National Patient organization dedicated to thrombosis and thrombophilia.
Today is Wednesday
And with that being said....TODAY IS STEPHANIE'S 10th Birthday. Happy Birthday Baby!!!
Also today is my 3 hr gestational diabetes test and growth ultrasound for Miabelle. Well it is currently 10:08 and I am waiting for my last blood draw at 10:40 before I get to grab something quick to eat and head to the ultrasound.
I am hoping she has gotten bigger and can not wait to see her again. That is about the only plus side to being considered high risk is the ultrasounds...but I would rather not get them and have a normal pregnancy.
Also today is my 3 hr gestational diabetes test and growth ultrasound for Miabelle. Well it is currently 10:08 and I am waiting for my last blood draw at 10:40 before I get to grab something quick to eat and head to the ultrasound.
I am hoping she has gotten bigger and can not wait to see her again. That is about the only plus side to being considered high risk is the ultrasounds...but I would rather not get them and have a normal pregnancy.
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