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Ullrich-Nielsen syndrome - translation to ρωσικά

CHROMOSOMAL DISORDER IN WHICH A FEMALE IS PARTIALLY OR COMPLETELY MISSING AN X CHROMOSOME

Turner's syndrome; Turner Syndrome; 45,X; XO syndrome; Turner's Syndrome; Gonadal dysgenesis Turner type; Bonnevie-Ullrich syndrome; Turners syndrome; Turners Syndrome; Karyotype 45,X; 45,X karyotype; Turner's; Turner disease; Ullrich-Turner syndrome; Bonnevie-Ulrich-Turner syndrome; Ulrich-Turner Syndrome; Bonnevie-Ullrich-Turner syndrome; Turner syndrome (Gonadal dysgenesis); Bonnevie Ullrich Turner syndrome; Single X syndrome; X syndrome; Bonnevie-Ulrich-Turner Syndrome; Bonnevie-Ulrich-Turner's Syndrome; Monosomy X; Partial anomalous venous drainage; Bonnevie–Ullrich–Turner syndrome; Bonnevie–Ullrich syndrome; Ring-X Turner Syndrome; Ring-X Turner syndrome; 45,X0

Ullrich-Nielsen syndrome

медицина

короткошейная врождённая дистрофия

врождённая дистрофия Нильсена

adiposogenital dystrophy

HYPOTHALAMIC DISEASE THAT IS CHARACTERIZED BY ENDOCRINE DYSFUNCTION OF THE HYPOTHALAMIC GLAND RESULTING IN DELAYED PUBERTY, SMALL TESTES, AND OBESITY

Babinski-Fröhlich syndrome; Fröhlich's syndrome; Froelich's syndrome; Frölich's Syndrome; Launois-Cleret syndrome; Frölich's syndrome; Frohlich's Syndrome; Froelich's Syndrome; Fröchlich syndrome; Dystrophia adiposogenitalis; Babinski-Fröhlich disease; Adiposogenital Dystrophy; Frolich's syndrome; Frolich's Syndrome; Frohlich's syndrome; Froehlich's syndrome; Babinski-Froehlich syndrome; Babinski-Frohlich syndrome; Babinski-Froehlich disease; Babinski-Frohlich disease; Frochlich syndrome; Froechlich syndrome; Babinski–Fröhlich syndrome

медицина

гипофизарный евнухоидизм

адипозогенитальная дистрофия

гипофизарное ожирение

cerebro-oculo-facio-skeletal syndrome

RARE AND FATAL AUTOSOMAL RECESSIVE NEURODEGENERATIVE DISORDER

Cockayne's syndrome; Neiill-Dingwall syndrome; Neill-Dingwall syndrome; Dwarfism-retinal atrophy-deafness syndrome; Cockayne syndrome type 1; Cockayne syndrome type 2; Cockayne syndrome type 3; Cerebrooculofacioskeletal Syndrome; Cockayne Syndrome type II; COFS syndrome; Pena Shokeir II syndrome; Pena Shokeir syndrome type II; Cerebrooculofacioskeletal syndrome; Pena-Shokeir syndrome, type 2; Cockayne syndrome type A; Cockayne syndrome type B; Cockayne syndrome type C; Cockayne syndrome type III; Cerebro-oculo-facio-skeletal syndrome; Cerebrooculofacioskeletal syndrome 1; Cerebrooculofacioskeletal syndrome 2; Cerebrooculofacioskeletal syndrome 4; Cofs syndrome; Type II Cockayne syndrome; Pena-Shokeir syndrome type II; Cocaine Syndrome; Cocaine syndrome

медицина

церебро-окуло-фациоскелетный синдром

Ορισμός

НИЛЬСЕН, КАРЛ АВГУСТ

(Nielsen, Carl August) (1865-1931), композитор, крупнейший представитель датского музыкального искусства. Родился 9 июня 1865 в Норре-Люндельсе на острове Фюн, в семье художника-любителя, который пополнял свой скудный бюджет игрой на деревенской скрипке и корнете.

В наследии Нильсена шесть симфоний, три концерта (для скрипки, флейты, кларнета), две оперы (Саул и Давид и Маскарад), множество сочинений камерных инструментальных жанров и большое собрание песен. Симфонии Нильсена, особенно Четвертая - Неугасаемая (1916) и Пятая (1922) - в числе лучших образцов этого жанра, созданных в 20 в.

Для Нильсена характерно новаторское отношение к тональности, при котором заключительная стадия всегда есть результат движения к тональному центру через ряд ладовых конфликтов и их разрешений. Таким образом достигается - с поразительной естественностью и тонкостью - качество, которое иногда называют "прогрессирующей тональностью". Можно сказать, что композитор раскрыл неиспользованные ресурсы тонального письма в эпоху, когда многим из его современников оно представлялось отжившим свой век. Умер Нильсен в Копенгагене 3 октября 1931.

Εμφάνιση περισσότερων ορισμών

Βικιπαίδεια

Turner syndrome

Turner syndrome (TS), also known as 45,X, or 45,X0, is a genetic disorder in which a female is partially or completely missing an X chromosome. Signs and symptoms vary among those affected. Often, a short and webbed neck, low-set ears, low hairline at the back of the neck, short stature, and swollen hands and feet are seen at birth. Typically, those affected do not develop menstrual periods, or breasts without hormone treatment and are unable to have children without reproductive technology. Heart defects, diabetes, and low thyroid hormone occur in the disorder more frequently than average. Most people with Turner syndrome have normal intelligence; however, many have problems with spatial visualization that may be needed in order to learn mathematics. Vision and hearing problems also occur more often than average.

Turner syndrome is not usually inherited; rather, it occurs during formation of the reproductive cells in a parent or in early cell division during development. No environmental risks are known, and the mother's age does not play a role. While most people have 46 chromosomes, people with Turner syndrome usually have 45 in some or all cells. The chromosomal abnormality is often present in just some cells, in which case it is known as Turner syndrome with mosaicism. In these cases the symptoms are usually fewer, and possibly none occur at all. Diagnosis is based on physical signs and genetic testing.

No cure for Turner syndrome is known. Treatment may help with symptoms. Human growth hormone injections during childhood may increase adult height. Estrogen replacement therapy can promote development of the breasts and hips. Medical care is often required to manage other health problems with which Turner syndrome is associated.

Turner syndrome occurs in between one in 2,000 and one in 5,000 females at birth. All regions of the world and cultures are affected about equally. Generally people with Turner syndrome have a shorter life expectancy, mostly due to heart problems and diabetes. American endocrinologist Henry Turner first described the condition in 1938. In 1964, it was determined to be due to a chromosomal abnormality.

https://en.wikipedia.org/wiki/Turner syndrome

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