- cri du chat disease
- Медицина: болезнь кошачьего крика (форма врождённой хромосомной патологии), синдром Лежена, синдром кошачьего крика
Универсальный англо-русский словарь. Академик.ру. 2011.
cri du chat disease
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Cri du chat — or Cri du chat Classification and external resources Facial features of a patient with Cri du Chat syndrome at age of 8 months (A), 2 years (B), 4 years (C) and 9 years (D) ICD 10 Q … Wikipedia
genetic disease, human — Introduction any of the diseases and disorders that are caused by mutations in one or more genes (gene). With the increasing ability to control infectious and nutritional diseases in developed countries, there has come the realization … Universalium
Maladie des griffes du chat — Cet article possède un paronyme, voir : Maladie du cri du chat. Maladie des griffes du chat Classification et ressources externes … Wikipédia en Français
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
Chromosome 5 (human) — Chromosome 5 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 5 spans about 181 million base pairs (the building blocks of DNA) and represents almost 6% of the total DNA in cells.… … Wikipedia
Список наследственных заболеваний — Список генетических заболеваний Основные статьи: наследственные заболевания, Наследственные болезни обмена веществ, Ферментопатия. В большинстве случаев приведен также код, указывающий на тип мутации и связанные с ней хромосомы. См. также система … Википедия
List of diseases (C) — A list of diseases in the English wikipedia.C* C syndrome * C1 esterase deficiency (angioedema)CaCac Cal* Cacchi Ricci disease * CACH syndrome * Cafe au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… … Wikipedia
Human genetics — describes the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics,… … Wikipedia
Telomerase — is an enzyme that adds specific DNA sequence repeats ( TTAGGG in all vertebrates) to the 3 ( three prime ) end of DNA strands in the telomere regions, which are found at the ends of eukaryotic chromosomes. The telomeres contain condensed DNA… … Wikipedia
Karyotype — A karyotype is the number and appearance of chromosomes in the nucleus of an eukaryotic cell. The term is also used for the complete set of chromosomes in a species, or an individual organism.[1][2]p28[3] Karyotypes describe the number of… … Wikipedia
List of congenital disorders — Numerical * 5p syndrome see Cri du chat A * Aicardi syndrome * Albinism * Amelia and hemimelia * Amniotic Band syndrome * Anencephaly * Angelman syndrome * Aposthia * Arnold Chiari malformation B * Bannayan Zonana syndrome * Bardet Biedl syndrome … Wikipedia
