synostosis$81208$ - traduction vers allemand
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synostosis$81208$ - traduction vers allemand

PREMATURE FUSION OF BONES IN THE SKULL
Craniostenosis; Craniostosis; Cranial synostosis; Craniostenoses; Craniosynostoses; Cloverleaf skull; Kleeblattschadel; Coronal synostosis; Cranial Stenosis; Kleeblattschädel; Primary craniosynostosis; Sagittal craniosynostosis syndrome; Warman–Mulliken–Hayward syndrome; Warman-Mulliken-Hayward syndrome; Metopic ridge; Lambdoid craniosynostosis
  • Kinds of craniosynostosis
  • Gene expression pattern during cranial suture fusion
  • Head of plagiocephalic baby viewed from above

synostosis      
n. Synostose, Knochenverwachsung
Klippel-Feil syndrome         
  • [[CT scan]] showing fused [[cervical vertebrae]] and [[Sprengel's deformity]] (arrow), as seen in Klippel–Feil syndrome
PHYSICAL DISORDER THAT HAS MATERIAL BASIS IN ABNORMAL SEGMENTATION OF THE VERTEBRA DURING FETAL DEVELOPMENT WHICH RESULTS IN FUSION LOCATED IN CERVICAL VERTEBRA
Klippel Feil syndrome; Klippel-Feil anomaly; Klippel-feil syndrome; Klippel Feil; Klippel Feil syndrome dominant type; Klippel Feil syndrome recessive type; Cervical vertebral fusion; Cervical vertebral fusion, congenital; Congenital cervical vertebral fusion; Fused cervical segments, congenital; Congenital fused cervical segments; Klippel-Feil malformation; Klippel-Feil sequence; Klippel-Feil deformity; Feil-Klippel syndrome; Klippel-Feil anomalad; Klippel-Feil phenotype; Klippel-Feil syndrome; Frontonasal dysplasia klippel feil syndrome; Frontonasal dysplasia Klippel–Feil syndrome; Short neck syndrome; Klippel–Feil syndrome recessive type; Klippel–Feil syndrome dominant type; Frontonasal dysplasia Klippel-Feil syndrome; Klippel-Feil syndrome dominant type; Klippel-Feil syndrome recessive type; Klippel Feil Syndrome; Klippel–Feil Syndrome; Klippel-Feil Syndrome; Andre Feil
n. Klippel-Feil-Syndrom, angeborenes Zusammenwachsen der Nackenwirbel und Abnormalitäten des Hirnstammes und des Kleinhirn (nach Andre Feil und Maurice Klippel die das Syndrom unabhängig voneinander in 1912 beschrieben)
Andre Feil         
  • [[CT scan]] showing fused [[cervical vertebrae]] and [[Sprengel's deformity]] (arrow), as seen in Klippel–Feil syndrome
PHYSICAL DISORDER THAT HAS MATERIAL BASIS IN ABNORMAL SEGMENTATION OF THE VERTEBRA DURING FETAL DEVELOPMENT WHICH RESULTS IN FUSION LOCATED IN CERVICAL VERTEBRA
Klippel Feil syndrome; Klippel-Feil anomaly; Klippel-feil syndrome; Klippel Feil; Klippel Feil syndrome dominant type; Klippel Feil syndrome recessive type; Cervical vertebral fusion; Cervical vertebral fusion, congenital; Congenital cervical vertebral fusion; Fused cervical segments, congenital; Congenital fused cervical segments; Klippel-Feil malformation; Klippel-Feil sequence; Klippel-Feil deformity; Feil-Klippel syndrome; Klippel-Feil anomalad; Klippel-Feil phenotype; Klippel-Feil syndrome; Frontonasal dysplasia klippel feil syndrome; Frontonasal dysplasia Klippel–Feil syndrome; Short neck syndrome; Klippel–Feil syndrome recessive type; Klippel–Feil syndrome dominant type; Frontonasal dysplasia Klippel-Feil syndrome; Klippel-Feil syndrome dominant type; Klippel-Feil syndrome recessive type; Klippel Feil Syndrome; Klippel–Feil Syndrome; Klippel-Feil Syndrome; Andre Feil
n. Andre Feil (1884-?), französischer Neurologe der in 1912 unabhängig von Maurice Klippel ein bestimmtes Syndrom beschrieb (heute Klippel-Feil Syndrom genannt)

Définition

Synostosis

Wikipédia

Craniosynostosis

Craniosynostosis is a condition in which one or more of the fibrous sutures in a young infant's skull prematurely fuses by turning into bone (ossification), thereby changing the growth pattern of the skull. Because the skull cannot expand perpendicular to the fused suture, it compensates by growing more in the direction parallel to the closed sutures. Sometimes the resulting growth pattern provides the necessary space for the growing brain, but results in an abnormal head shape and abnormal facial features. In cases in which the compensation does not effectively provide enough space for the growing brain, craniosynostosis results in increased intracranial pressure leading possibly to visual impairment, sleeping impairment, eating difficulties, or an impairment of mental development combined with a significant reduction in IQ.

Craniosynostosis occurs in one in 2000 births. Craniosynostosis is part of a syndrome in 15% to 40% of affected patients, but it usually occurs as an isolated condition. The term is from cranio, cranium; + syn, together; + ost, relating to bone; + osis, denoting a condition.