A female with a gene for a genetic disorder will usually only have it on one of her two X chromosomes. The other chromosome will carry the healthy version of the gene, which will carry out that gene's function when the other chromosome cannot. Males will exhibit the disease if they have the gene as a male human only has one X chromosome. So, in order for a female to have a genetic disorder carried on her sex chromosome her mother would have to have the defective gene and her father would have the disorder.
Both X chromosomes must carry the recessive trait. Since males only have one X chromosome, it is much easier for males to have the recessive phenotype. Put another way, a female would have to receive an X chromosome with the recessive gene from both parents, which would mean the father already displays the recessive disorder.
Yes, female yaks can have horns, but they are usually smaller than the horns of male yaks.
color blindness is one
In a typical setting, one male turkey is usually kept with around 5-10 female turkeys.
This condition is known as Persistent Müllerian Duct Syndrome (PMDS) or male pseudohermaphroditism. It is a rare genetic disorder where individuals with male chromosomes (XY) have both male internal reproductive organs (testes) and female reproductive structures (fallopian tubes and uterus).
Usually female.
Some female carriers of Fabry's disease show mild signs of the disorder, especially cloudiness of the cornea.
Haemophilia is a sex-linked recessive disorder - which means it can skip a generation, but only if it is carried in the female line.A female can be a carrier of haemophilia, but a male cannot. This is because males only have one X chromosome, so if they have a defective X they will have the disorder. If a father has haemophilia, all of his daughters will also have haemophilia.
wheat disorder female
Sickle cell disease is an autosomal reccessive sexlinked trait so, a female msut have 2 recessive alleles to have the trait and a male needs only one allele (this is because there is no corresponding site for this allele on the Y chromosome. The female can be a carrier of the disorder with the defective allele on one X chromosome and a normal allele on the other X chromosome. Female carrriers can have a mixture of normal and abnormal redblood cells.
Anorexia appear in roughly 1 out of every 250 to 300 people. Of that, one male is affected for every female affected with the eating disorder. Anorexia usually occurs between the ages of roughly 12 and 25.
.usually begins before the age of 30. 0.2% of the United States population will develop this disorder. 1% of all women in the United States have symptoms of this disorder. The female-to-male ratio is estimated to range between 5:1 and 20:1.
The population of the United States of America are mostly affected by Binge Eating Disorder.
You might need to indicate what the disorder is.
Anyone can be a carrier of a recessive genetic disorder (as long as it is not associated with the sex chromosomes) no matter what their gender since "carrier" refers to an individual that is heterozygous for the recessive allele and therefore phenotypically normal. Specifically, sexlinked genetic disorders can be "carried" by a heterozygous female but males (having only one X chromosome) cannot. Males will either be free of the defective gene or be affected.
Turner's Syndrome
Common female sexual dysfunctions include: Female sexual interest/arousal disorder, which is characterized by a lack of sexual desire or difficulty in becoming sexually aroused. Female orgasmic disorder, where a woman has difficulty experiencing orgasm or is unable to orgasm. Genito-pelvic pain/penetration disorder, which involves pain during sexual intercourse or difficulty with vaginal penetration. Dyspareunia, which is recurrent or persistent genital pain before, during, or after sexual intercourse.