Turner syndrome: Description Turner syndrome is also known as monosomy X. It occurs in one in 2,500 newborns. Women with Turner syndrome lack functioning ovaries. Turner syndrome is called a syndrome because there are several signs of the disease that occur at the same time and are related. It is also referred to as a … Turner Syndrome: Symptoms, Treatment
Brachymetatarsia is a shortening of the metatarsal bone that is already congenital. It represents a form of brachyphalangia. What is brachymetatarsia? Brachymetatarsia is a deformity of the foot. In this case, the length growth of the metatarsal bone is stopped at an early stage. In most cases, the 1st and 4th metatarsal bones are affected … Brachymetatarsia: Causes, Symptoms & Treatment
Turner syndrome or Ullrich-Turner syndrome is due to an X chromosomal abnormality that manifests primarily by short stature and failure to reach puberty. Turner syndrome affects almost exclusively girls (about 1 in 3000). What is Turner syndrome? Turner syndrome is the name given to a gonadal dysgenesis (absence of functional germ cells) that is usually … Turner Syndrome: Causes, Symptoms & Treatment
Hermaphroditism, also called hermaphroditism or hermaphroditism, refers to individuals who cannot be clearly assigned to one sex genetically, anatomically or hormonally. Today, however, the term intersexuality is more commonly used for this medical phenomenon. Intersexuality belongs to the sexual differentiation disorders. The German Institute of Medical Documentation and Information (DIMDI) (ICD-10-GM-2018) classifies this form in … Hermaphroditism
There are people who cannot be clearly assigned to any gender. They carry characteristics of both sexes and fall under the term intersexuality. In Greek mythology, they were called hermaphrodites. What is intersexuality? The term intersexuality stands for a constellation in which physical predispositions for both sexes are found in people and therefore they cannot … Intersexuality: Causes, Symptoms & Treatment
Gametes are the fertilizable male and female gametes or germ cells. Their diploid (twofold) set of chromosomes has been reduced to a haploid (single) set by prior meiosis (maturation division), resulting in a diploid cell with a twofold set of chromosomes after fertilization, the union of a female and a male gamete. The female gamete … Gamete: Structure, Function & Diseases
Chromosomes are the transmitters of genetic information. They ensure that physical characteristics of the parents are passed on to their common children. At the same time, serious diseases can occur when chromosomes are disrupted. What are chromosomes? DNA are the basis for heredity. This is present rolled up in the form of chromosomes. Humans have … Chromosomes: Structure, Function & Diseases
Definition – what is the Turner syndrome? Turner syndrome, also known as Monosomy X and Ullrich-Turner syndrome, is a genetic disorder that affects only girls. It was named after its discoverers, the German pediatrician Otto Ullrich and the American endocrinologist Henry H. Turner. Characteristic signs of the Turner syndrome are dwarfism and infertility. Turner syndrome … Turner Syndrome
I recognize a Turner syndrome by these symptoms There are a number of possible symptoms that can occur in Turner syndrome. However, these do not all occur simultaneously. Some symptoms can also be age-related. Already at birth, newborns are conspicuous by lymphedema of the backs of the hands and feet. The dwarfism is also noticed … I recognize a Turner syndrome by these symptoms | Turner Syndrome
Duration Prognosis Since the Turner syndrome is not curable, girls and women affected by the disease are accompanied by the disease throughout their lives. A regular medical examination is important, as there is an increased risk of various diseases. These include: High blood pressure, diabetes mellitus, overweight, osteoporosis, diseases of the thyroid gland and diseases … Duration Prognosis | Turner Syndrome
