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Chondrodysplasia punctata Toriello type
Giant cell chondrodysplasia
Metaphyseal chondrodysplasia Kaitila type

Translation of "chondrodysplasia " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Chondrodysplasia punctata Toriello type

syndrome de Toriello-Higgins-Miller
SNOMEDCT-BE (disorder) / 715631005
SNOMEDCT-BE (disorder) / 715631005


Chondrodysplasia punctata, MT type

chondrodysplasie ponctuée tibio-métacarpienne
SNOMEDCT-BE (disorder) / 254083002
SNOMEDCT-BE (disorder) / 254083002


Parastremmatic dwarfism is a very rare chondrodysplasia with characteristics of severe dwarfism, kyphoscoliosis, stiffness of large joints and distortion of lower limbs. Radiographs show bowing of long bones, platyspondyly and a very rough, irregular

nanisme parastremmatique
SNOMEDCT-BE (disorder) / 722210007
SNOMEDCT-BE (disorder) / 722210007


Metaphyseal chondrodysplasia Kaitila type

chondrodysplasie métaphysaire type Kaitila
SNOMEDCT-BE (disorder) / 770909004
SNOMEDCT-BE (disorder) / 770909004


An extremely rare disorder of sex development, reported in only two siblings to date. The syndrome has clinical features of 46,XY complete gonadal dysgenesis in association with severe dwarfism with generalised chondrodysplasia (bell-shaped thorax, m

syndrome de chondrodysplasie-anomalie du développement sexuel
SNOMEDCT-BE (bell-shaped thorax, m / 720851007
SNOMEDCT-BE (disorder) / 720851007


A rare genetic bone disorder with characteristics of chondrodysplasia, intrauterine growth retardation, hydrocephaly and facial dysmorphism in the affected males. The disease is severe and probably lethal in males, the clinical picture in females is

chondrodysplasie dominante liée à l'X type Chassaing-Lacombe
SNOMEDCT-BE (disorder) / 719837003
SNOMEDCT-BE (disorder) / 719837003


Giant cell chondrodysplasia

atélostéogenèse type I
SNOMEDCT-BE (disorder) / 725141006
SNOMEDCT-BE (disorder) / 725141006


A form of non-rhizomelic chondrodysplasia punctata, a primary bone dysplasia, with characteristics of hypoplasia of the distal phalanges of the fingers, nasal hypoplasia, epiphyseal stippling appearing in the first year of life, as well as mild and n

chondrodysplasie ponctuée avec brachytéléphalangie
SNOMEDCT-BE (disorder) / 778067002
SNOMEDCT-BE (disorder) / 778067002


An extremely rare lethal form of chondrodysplasia with characteristics of severe micromelic dwarfism, short and incurved limbs with normal hands and feet, facial dysmorphism (disproportionately large skull, frontal prominence, slightly flattened nasa

chondrodysplasie létale autosomique récessive
SNOMEDCT-BE (disproportionately large skull, frontal prominence, slightly flattened nasa / 719404009
SNOMEDCT-BE (disorder) / 719404009


Metaphyseal chondrodysplasia, Spahr type

chondrodysplasie métaphysaire type Spahr
SNOMEDCT-BE (disorder) / 254084008
SNOMEDCT-BE (disorder) / 254084008
IN-CONTEXT TRANSLATIONS
For many rare diseases, signs may be observed at birth or in childhood, as in proximal spinal muscular atrophy, neurofibromatosis, osteogenesis imperfecta, chondrodysplasia or Rett syndrome.

On peut observer les signes à la naissance ou durant l'enfance pour de nombreuses maladies rares, notamment l'amyotrophie spinale proximale, la neurofibromatose, l'ostéogenèse imparfaite, la chondrodysplasie ou le syndrome de Rett.




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'chondrodysplasia'

Date index:2022-03-27 -

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