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Multiple congenital anomalies

Translation of "multiple congenital anomalies " (English → French) :

TERMINOLOGY
see also In-Context Translations below
A rare multiple congenital anomalies syndrome with characteristics of mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax
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syndrome cranio-facio-fronto-digital
SNOMEDCT-BE (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax / 763320005
SNOMEDCT-BE (disorder) / 763320005
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https://browser.ihtsdotools.or (...) [HTML]
A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of male, 46,XY gonadal dysgenesis, cleft palate, micrognathia, conotruncal heart defects and unspecific skeletal, brain and kidney anomalies.
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syndrome génito-palato-cardiaque
SNOMEDCT-BE (disorder) / 773749003
SNOMEDCT-BE (disorder) / 773749003
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https://browser.ihtsdotools.or (...) [HTML]
A multiple congenital anomalies/dysmorphic syndrome with characteristics of multiple skeletal malformations (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t
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syndrome de Verloove-Van Horick-Brubakk
SNOMEDCT-BE (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t / 764697003
SNOMEDCT-BE (disorder) / 764697003
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https://browser.ihtsdotools.or (...) [HTML]
Multiple congenital anomalies
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syndrome de malformation congénitale
SNOMEDCT-BE (disorder) / 400038003
SNOMEDCT-BE (disorder) / 400038003
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https://browser.ihtsdotools.or (...) [HTML]
A multiple congenital anomalies syndrome characterized by moderate postnatal overgrowth, macrocephaly, craniofacial dysmorphism (including high forehead and anterior hairline, downslanting palpebral fissures, prominent chin), developmental delay, and
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syndrome de croissance excessive de Malan
SNOMEDCT-BE (including high forehead and anterior hairline, downslanting palpebral fissures, prominent chin), developmental delay, and / 763795006
SNOMEDCT-BE (disorder) / 763795006
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Belongs to the group of multiple congenital anomalies/mental retardation syndromes with intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def
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syndrome de McDonough
SNOMEDCT-BE (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def / 715441004
SNOMEDCT-BE (disorder) / 715441004
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https://browser.ihtsdotools.or (...) [HTML]
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
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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
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https://browser.ihtsdotools.or (...) [HTML]
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of cerebellar-like ataxia, photosensitivity (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin
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syndrome d'ataxie-photosensibilité-petite taille
SNOMEDCT-BE (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin / 773769008
SNOMEDCT-BE (disorder) / 773769008
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https://browser.ihtsdotools.or (...) [HTML]
A very rare multiple congenital anomalies syndrome described in three brothers of one South-African family, and with features of hypospadias and intellectual deficit, in association with microcephaly, craniofacial dysmorphism, joint laxity and beaked
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syndrome d'hypospadias-déficience intellectuelle type Goldblatt
SNOMEDCT-BE (disorder) / 716096005
SNOMEDCT-BE (disorder) / 716096005
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Limb body wall complex (LBWC) is a syndrome with features of severe multiple congenital anomalies. Clinical manifestations vary widely and include limb defects and visceral malformations, spinal abnormalities, absent diaphragm, bowel atresia and rena
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syndrome LBWC (limb body wall complex)
SNOMEDCT-BE (disorder) / 716106000
SNOMEDCT-BE (disorder) / 716106000
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IN-CONTEXT TRANSLATIONS
Table 1: ICD-10-CA codes used to determine congenital anomalies, diseases of prematurity, multiple births and stillbirths among singleton live-born newborns, Ontario, 2007–09
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Tableau 1 : Codes CIM-10-CA utilisés pour déterminer les anomalies congénitales, les maladies de la prématurité, les naissances multiples et les mortinaissances dans l’étude portant sur les nouveau-nés vivants issus d’une grossesse unique, Ontario, 2007 à 2009
http://www.phac-aspc.gc.ca/pub (...) (...) [HTML]
http://www.phac-aspc.gc.ca/pub (...) [HTML]
Fetal and Infant Health Outcomes Preterm Birth Rate Postterm Birth Rate Small-for-Gestational-Age Rate Large-for-Gestational-Age Rate Fetal Mortality Rate Infant Mortality Rate and Causes of Death Severe Neonatal Morbidity Rate Multiple Birth Rate Prevalence of Congenital Anomalies Rate of Neonatal Hospital Readmission after Discharge following Birth
http://www.phac-aspc.gc.ca/rhs (...) (...) [HTML]
Répercussions sur la santé foetale et infantile Taux de prématurité Taux de postmaturité Taux d'hypotrophie néonatale Taux d'hypertrophie néonatale Taux de mortalité foetale Taux de mortalité infantile et causes de décès Taux de morbidité néonatale grave Taux d'accouchement multiple Prévalence des anomalies congénitales Taux de réadmission des nouveau-nés après le congé de l'hôpital
http://www.phac-aspc.gc.ca/rhs (...) (...) [HTML]
http://www.phac-aspc.gc.ca/rhs (...) [HTML]


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Date index:2022-06-26 -

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