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Arnold-Chiari malformation
Cerebellar ectopia
Chiari malformation
Congenital absence of vertebra
Fusion of spine
Hemivertebra
Hereditary malformation
Herniation of the cerebellar tonsils
Hindbrain herniation
Infants
Kyphosis
Lordosis
Malformation of lumbosacral
Malformation of spine
Malformation of the bladder
Mondini's malformation
Platyspondylisis
Prenatal malformation
Primary
Supernumerary vertebra
Unspecified or not associated with scoliosis
Vesical malformation

Translation of "Mondini's malformation " (English → French) :

Mondini's malformation

malformation de Mondini
The Ear
Oreille


Arnold-Chiari malformation | cerebellar ectopia | Chiari malformation | herniation of the cerebellar tonsils | hindbrain herniation

malformation d'Arnold-Chiari
IATE - Health
IATE - Health


hereditary malformation | prenatal malformation

malformation déficitaire
IATE - Health
IATE - Health


malformation of the bladder | vesical malformation

malformation vésicale
IATE - Health
IATE - Health


A unique form of congenital adrenal hyperplasia characterised by glucocorticoid deficiency, severe sexual ambiguity in both sexes and skeletal (especially craniofacial) malformations. Prenatal androgen excess is responsible for severe virilisation of

hyperplasie congénitale des surrénales par déficit en cytochrome P450 oxydoréductase
SNOMEDCT-BE (especially craniofacial) malformations. Prenatal androgen excess is responsible for severe virilisation of / 715733000
SNOMEDCT-BE (disorder) / 715733000


A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are intellectual disability, growth and developmental delay, facial dysmorphism (including microphthalmia, deep-set eyes, low-set, malformed ears, bulbous

trisomie 9 en mosaïque
SNOMEDCT-BE (including microphthalmia, deep-set eyes, low-set, malformed ears, bulbous / 764989007
SNOMEDCT-BE (disorder) / 764989007


Congenital:absence of vertebra | fusion of spine | kyphosis | lordosis | malformation of lumbosacral (joint) (region) | Hemivertebra | Malformation of spine | Platyspondylisis | Supernumerary vertebra | unspecified or not associated with scoliosis

Absence congénitale de vertèbres | Cyphose congénitale | Hémivertèbre [hémispondylie] | Lordose congénitale | Malformation congénitale (charnière) de la région lombo-sacrée | Malformation du rachis | Platyspondylie | Synostose vertébrale congénitale | Vertèbre surnuméraire | sans précision ou non associée à une scoliose
WORLD HEALTH ORGANIZATION ICD-10: Q76.4
WORLD HEALTH ORGANIZATION ICD-10: Q76.4


A rare genetic multiple congenital anomalies syndrome with characteristics of second branchial arch anomalies (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing

syndrome branchio-otique
SNOMEDCT-BE (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing / 764810000
SNOMEDCT-BE (disorder) / 764810000


Aplasia, (pure) red cell (of):congenital | infants | primary | Blackfan-Diamond syndrome Familial hypoplastic anaemia Fanconi's anaemia Pancytopenia with malformations

Anémie (de):Fanconi | hypoplasique familiale | Erythroblastopénie (pure) (du):congénitale | nourrisson | primaire | Pancytopénie avec malformations Syndrome de Blackfan-Diamond
WORLD HEALTH ORGANIZATION ICD-10: D61.0
WORLD HEALTH ORGANIZATION ICD-10: D61.0


Meningeal haemorrhage Rupture of cerebral arteriovenous malformation

Hémorragie méningée Rupture d'une malformation artérioveineuse cérébrale
WORLD HEALTH ORGANIZATION ICD-10: I60.8
WORLD HEALTH ORGANIZATION ICD-10: I60.8




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Mondini's malformation

Date index:2023-07-09 -

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