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Absence
Aortic arch
Aortic arch syndrome
Aplasia
Arch of aorta
Arch of aorta-syndrome
Arch of the aorta
Arcus aortae
Congenital aneurysm
Dilatation
Of aorta
Pulseless disease
Right aortic arch
Right arch of aorta
Takayasu
Tranverse aorta
Vascular ring of aorta

Translation of "arch aorta-syndrome " (English → French) :

arch of aorta-syndrome | pulseless disease

maladie sans pouls | syndrome de la crosse de l'aorte | syndrome de Martorell
IATE - Health
IATE - Health


arch of the aorta | arch of aorta | aortic arch | arcus aortae

arc de l'aorte
médecine > anatomie | médecine > cardiologie
médecine > anatomie | médecine > cardiologie


arch of aorta [ aortic arch | tranverse aorta | arcus aortae ]

crosse de l'aorte [ crosse aortique | arc de l'aorte | arcus aortae ]
Vessels (Medicine)
Vaisseaux (Médecine)


Absence | Aplasia | Congenital:aneurysm | dilatation | of aorta | Aneurysm of sinus of Valsalva (ruptured) Double aortic arch [vascular ring of aorta] Hypoplasia of aorta Persistent:convolutions of aortic arch | right aortic arch

Absence | Anévrisme | Dilatation | Aplasie | congénital(e) | de l'aorte | Anévrisme du sinus de Valsalva (rompu) Double arc aortique [anneau vasculaire de l'aorte] Hypoplasie de l'aorte Persistance de:arc aortique droit | convolution de l'arc aortique
WORLD HEALTH ORGANIZATION ICD-10: Q25.4
WORLD HEALTH ORGANIZATION ICD-10: Q25.4


right arch of aorta

crosse de l'aorte en dextro-position
IATE - Health
IATE - Health


arch of aorta

crosse de l'aorte
IATE - Health
IATE - Health


This syndrome has characteristics of severe short stature with disproportionately short legs, small hands, clinodactyly, valvular heart disease and dysmorphism (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and tw

syndrome de petite taille-valvulopathie cardiaque-dysmorphie
SNOMEDCT-BE (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and tw / 716193004
SNOMEDCT-BE (disorder) / 716193004


A rare cardiovascular morphological anomaly due to maldevelopment of embryonal aorta resulting in right aortic arch and left ligamentum arteriosum characterized by tracheoesophageal compression symptoms (stridor, dyspnea, dysphagia, apneic episodes,

anomalie de Neuhauser
SNOMEDCT-BE (stridor, dyspnea, dysphagia, apneic episodes, / 766751007
SNOMEDCT-BE (disorder) / 766751007


Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome

syndrome d'arc aortique anormal-dysmorphie-déficience intellectuelle
SNOMEDCT-BE (disorder) / 763615003
SNOMEDCT-BE (disorder) / 763615003


Aortic arch syndrome [Takayasu]

Syndrome de la crosse aortique [Takayasu]
WORLD HEALTH ORGANIZATION ICD-10: M31.4
WORLD HEALTH ORGANIZATION ICD-10: M31.4




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'arch aorta-syndrome'

Date index:2022-06-29 -

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