that hormone is Testosterone. It is male sex hormone
Male hemophiliacs inherit it from their mother, because hemophilia is only on the X gene and males only have one and it is from their mother.
There are actually a bunch of different hormones that cause the changes during puberty, but the dominant one in males is testosterone, while the dominant one in females is estrogen.
estrogen, testosterone is in males.
Estrogen
Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.
affects males and females of all ethnic groups. It is estimated that there are about one in 4,000 to one in 6,250 males affected with fragile X syndrome. There are approximately one-half as many females with fragile X syndrome as there are males
Human papillomavirus (HPV) is a virus that affects both males and females, and its origins are not specifically tied to one gender. It is believed to have evolved alongside humans over thousands of years. HPV is primarily transmitted through intimate skin-to-skin contact, and both sexes can carry and spread the virus. Therefore, it is not accurate to attribute the origin of HPV to either males or females specifically.
The hypothalamus is linked to the pituitary gland, which controls the release of many hormones, including the one that develops the sex organs.
Person having klinefelter's syndrome disorder have risk of developing breast cancer and osteoporosis as it affects one out of 500-1000 newborn males
Hormone secretions are primarily regulated by three mechanisms: feedback systems, particularly negative feedback, which maintain homeostasis by adjusting hormone levels in response to changes in the body; hormonal regulation, where one hormone stimulates or inhibits the secretion of another hormone; and neural regulation, where the nervous system directly influences hormone release through nerve impulses. Together, these mechanisms ensure precise control of hormone levels to support bodily functions.
Duchenne muscular dystrophy (DMD) is inherited in an X-linked recessive pattern, which primarily affects males. The condition is caused by mutations in the dystrophin gene located on the X chromosome. Since males have one X and one Y chromosome, a single mutated copy of the gene leads to the development of the disease. Females, having two X chromosomes, can be carriers if they have one mutated gene but typically do not show symptoms unless both X chromosomes carry the mutation.
Yes, hemophilia is a sex-linked disorder, specifically linked to the X chromosome. It primarily affects males, as they have only one X chromosome; if that chromosome carries the mutation, they will express the disorder. Females, having two X chromosomes, can be carriers of the hemophilia gene without necessarily exhibiting symptoms, as they may have one normal X chromosome that compensates for the defective one.