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D014807. Legal status. In Wikidata. Vitamin D is a group of fat-soluble secosteroids responsible for increasing intestinal absorption of calcium, magnesium, and phosphate, and for many other biological effects. [1] [2] [3] In humans, the most important compounds in this group are vitamin D 3 ( cholecalciferol) and vitamin D 2 ( ergocalciferol ).
Definition. Deficiency. Medical uses. Dietary recommendations. Sources. Drug interactions. Chemistry. Biochemistry. Physiology. Synthesis. History. Society and culture. See also. Further reading. References. External links. Vitamin B 12. Vitamin B12, also known as cobalamin, is a water-soluble vitamin involved in metabolism. [2] .
Stockholm syndrome. Former Kreditbanken building in Stockholm, Sweden, the location of the 1973 Norrmalmstorg robbery (photographed in 2005) Stockholm syndrome is a proposed condition or theory that tries to explain why hostages sometimes develop a psychological bond with their captors. [1] [2] It is supposed to result from a rather specific ...
Klinefelter syndrome ( KS ), also known as 47,XXY, is a chromosome anomaly where a male has an extra X chromosome. [10] These complications commonly include infertility and small, poorly functioning testicles (if present). These symptoms are often noticed only at puberty, although this is one of the most common chromosomal disorders, occurring ...
Asperger syndrome (AS), also known as Asperger's syndrome or Asperger's, is a term formerly used to describe a neurodevelopmental disorder characterized by significant difficulties in social interaction and nonverbal communication, along with restricted, repetitive patterns of behavior and interests.[5] Asperger syndrome has been merged with ...
Turner syndrome. Turner syndrome ( TS ), also known as 45,X, or 45,X0, is a genetic disorder in which a person's cells have only one X chromosome or are partially missing an X chromosome ( sex chromosome monosomy ). [2] [6] Most people have two sex chromosomes (XX or XY). The chromosomal abnormality is often present in just some cells, in which ...
Williams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body.[2] Facial features frequently include a broad forehead, underdeveloped chin, short nose, and full cheeks.[2] Mild to moderate intellectual disability is observed in people with WS, with particular challenges with visual ...
