- chondrodysplasia
- chondrodysplasia.См. хондродисплазии.(Источник: «Англо-русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд-во ВНИРО, 1995 г.)
.
.
Chondrodysplasia punctata — Classification and external resources ICD 10 Q77.3 DiseasesDB 32527 … Wikipedia
Chondrodysplasia punctata — Klassifikation nach ICD 10 Q77.3 Chondrodysplasia punctata Syndrome … Deutsch Wikipedia
chondrodysplasia — noun A genetic disorder characterized by short limbed dwarfism … Wiktionary
chondrodysplasia — SYN: chondrodystrophy. [chondro + G. dys, bad, + plasis, a molding] c. calcificans congenita [MIM*118650] autosomal dominant inheritance characterized by asymmetric calcifications and dysplastic skeletal changes, less frequent occurrence of… … Medical dictionary
Chondrodysplasia — Chon|dro|dys|pla̱sia* [↑chondro... u. ↑Dysplasie] w; , ...iae; in der Fügung: Chon|dro|dys|pla̱sia mala̱cica: Wachstumsstörung mit schleimiger Erweichung des Knorpelgewebes … Das Wörterbuch medizinischer Fachausdrücke
chondrodysplasia — chon·dro·dys·pla·sia … English syllables
chondrodysplasia — chondro osteodystrophy; = chondrodystrophy; n. any of various conditions in which there is abnormal cartilage development. It affects long bones and can cause short limb dwarfism, overgrowth of the epiphysis, or other deformities. One particular… … The new mediacal dictionary
chondrodysplasia — | ̷ ̷ ̷ ̷də̇ˈsplāzh(ē)ə noun ( s) Etymology: New Latin, from chondr + dys + plasia : a hereditary skeletal disorder characterized by the formation of exostoses at the epiphyses and resulting in arrested development and deformity called also… … Useful english dictionary
Chondrodysplasia, metaphyseal (McKusick type) — Also known as cartilage hair hypoplasia syndrome, this is a specific genetic form of short limbed dwarfism with skeletal features that also include normal head, inability to fully extends the elbows, chest cage deformity, bow legs (genu varum),… … Medical dictionary
chondrodysplasia punctata — a heterogeneous group of bone dysplasias whose common characteristic is stippling of the epiphyses in infancy. There are a severe autosomal recessive form (rhizomelic dwarfism), an autosomal dominant form (Conradi HÑŒnermann syndrome), and a… … Medical dictionary