What is Toulouse-Lautrec syndrome

Toulouse-Lautrec syndrome

Toulouse-Lautrec syndrome is diagnosed in the late 19th-century French painter Henry de Toulouse-Lautrec (1952 by Jose Ferrer '' Moulin Rouge ').

Toulouse-Lautrec syndrome is a genetic (inherited) disease of the bone. Its inherited pattern follows the classical laws of genetics (see below).

Toulouse-Lautrec syndrome is often caused by a short condition. Adult males with the disease are less than 150 centimeters (59 inches or 4 feet 11 inches) tall. Adult females with pycnodysostosis are even shorter.

Toulouse-Lautrec syndrome causes bone abnormally ensemble (osteosclerosis); The last bones of the fingers (distal phalanges) should be abnormally short; In infancy, the contours (sutures) of the skull usually delay closing, leaving the "soft spot" (fontanelle) above the head wide open.

Toulouse-Lautrec syndrome is easily broken by fractures (fractures). The bones in the legs and feet tend to break. The jaw and neck bones (clavicles) are also particularly prone to fractures.

The exact frequency of Toulouse-Lautrec syndrome has never been determined. Pycnodystosis can be broadly classified as a group of genetic diseases, but they are collectively important because of the combination of their numbers, the high impact they have on affected individuals, and the burden they place on their families.