- Albright’s syndrome
- Медицина: синдром Олбрайта (Олбрайта наследственная остеодистрофия)
Универсальный англо-русский словарь. Академик.ру. 2011.
Универсальный англо-русский словарь. Академик.ру. 2011.
Syndrome de Klinefelter — Classification et ressources externes Les personnes atteintes d un syndrome de Klinefelter ont un chromosome X supplémentaire, leur caryotype est 47,XX … Wikipédia en Français
Albright syndrome — Albright syndrome. См. псевдогипопаратиреоз. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
Albright syndrome — 1. A genetic disorder of bones, skin pigmentation and hormonal problems with premature sexual development. Also called McCune Albright syndrome and polyostotic fibrous dysplasia. In the syndrome, there is bone disease with fractures and deformity … Medical dictionary
Albright-Syndrom — Fibröse Dysplasie ist eine chronische Fehlbildung des Knochens, bei der der Knochen nicht in seiner üblichen Zellstruktur wächst, sondern geschwulstartige Auswüchse mit unregelmäßiger Zellstruktur bildet. Es handelt sich dabei wie bei allen… … Deutsch Wikipedia
Albright's hereditary osteodystrophy — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 10835 ICD10 = ICD10|E|20|1|e|20 ICD9 = ICD9|275.49 ICDO = OMIM = 103580 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D005359 Albright hereditary osteodystrophy (or Martin Albright… … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Albright hereditary osteodystrophy syndrome — Al·bright hereditary osteodystrophy, syndrome (awlґbrīt) [Fuller Albright, American physician and endocrinologist, 1900–1969] see pseudohypoparathyroidism and see under syndrome … Medical dictionary
Syndrome, Klinefelter — A chromosome condition in boys and men that is usually due to their having 47 chromosomes with XXY sex chromosomes, rather than having the usual 46 chromosomes with XY sex chromosomes. XXY is one of the most common chromosomal abnormalities. It… … Medical dictionary
Albright — Fuller, U.S. physician, 1900–1969. See A. disease, A. syndrome, A. hereditary osteodystrophy, Forbes A. syndrome, McCune A. syndrome … Medical dictionary
Albright dystrophy — see under syndrome … Medical dictionary
Klinefelter's syndrome — Infobox Disease ICD10 = ICD10|Q|98|0|q|90 ICD10|Q|98|4|q|90 ICD9 = ICD9|758.7 Caption = 47,XXY ICDO = OMIM = MedlinePlus = eMedicineSubj = ped eMedicineTopic = 1252 MeshID = D007713 Klinefelter s syndrome, 47,XXY or XXY syndrome is a condition… … Wikipedia