Doctor insights on:
Is Ethnicity A Factor In Antiphospholipid Syndrome
Metabolic syndrome is a risk factor for:: Brachial plexus injury, Erectile dysfunction, Essential hypertension, Rhabdomyolysis, Heart attack, BPH, ST elevation myocardial infarction, Polycystic ovary syndrome, High blood pressure, Fatty liver, Acanthosis nigricans, Endometrial cancer, Hypertriglyceridemia, Male pattern baldness, Metabolic syndrome. ...Read more
Depends on which : Factor. There are about a dozen clotting factors and any of those could be deficient. Some are serious others not so much. It is not feasible to provide specific suggestion from the information provided. ...Read more
Not usually: On www.Angelman.Org there is an explanation of the ways in which the genetic errors that cause angelman syndrome can occur.In a very few cases, there is an alteration in mother's ub3a gene or a balanced translocation on her chromosome 15 that increases risk, but usually it's a new mutation. ...Read more
Yes: Some epilepsies are clearly genetic- many of these are a type of generalized epilepsy (seizures start both sides of the brain at the same time). Less commonly, some partial epilepsies may be genetic (seizures from one part of the brain). Even some acquired forms of epilepsy may have a genetic component- such as epilepsy secondary to head trauma (though not in every case). ...Read moreSee 1 more doctor answer
Pregnancy outcome: Individuals with antiphospholipid syndrome may be at an increased risk of first trimester recurrent pregnancy loss. Treatments are available though to improve outcome. Make sure your OB or your fertility specialist knows so he/she can address appropriately. ...Read moreSee 2 more doctor answers
Is there evidence that a mutation in a single gene causes combined factors v and viii deficiency?
Factor v viii def: Good wikipedia question.Get a more detailed answer ›
More info: Pathogenic is a medical worse for disease causing. Genetic disorders cause disease processes that can be considered pathogenic. More information is needed for me to help you. ...Read more
Is their a gene specifically associated with the hypermobile form of ehleres- danlos syndrome? And is it one that is able to be tested ?
See geneticist!: Type 3: hypermobility form - ehlers-danlos is caused by an autosomal dominant or recessive mechanism. Mutations in either of two separate genes (which are also involved in vascular eds and tenascin-x deficiency eds, respectively) may lead to this variant. Tnxb sequencing or quantitative serum tenascin-x analysis or testing of eds-associated genes, especially col3a1can be done. ...Read moreSee 2 more doctor answers
Miscarriage: Apa, along with lupus anti-coagulant antibody, are two antibodies that attack the areas in the cell wall of growing tissue, especially the fast-growing placental tissue of an early pregnancy. These are newly-discovered causes for recurrent miscarriage, and are usually treated with Heparin injections and Aspirin during pregnancy. ...Read more
Is fetal alcohol syndrome hereditary or is there a hereditary disposition associated with getting it?
Disease not herited: DRESS is short for Drug Reaction with Eosinophilia Systemic Symptoms meaning usually caused by certain drugs with rashes, elevation of some body enzymes, and other blood abnormalities. Usually rashes and abnormalities disappear when the offending drug is stopped but some do progress. ...Read more
Would a diagnosis of the VASCULAR subtype of Ehlers-Danlos syndrome likely happen before age 35? Hypermobile family with no sudden deaths.
It can: I have seen it but it sounds unlikely in you. ...Read more
No statistics: It is a rare disease in anyone. ...Read more
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