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Arnold-Chiari malformation
Cerebellar ectopia
Chiari I herniation
Chiari I malformation
Chiari malformation
Chiari malformation type I
Congenital absence of vertebra
Dysgenesis
Fusion of spine
Hemivertebra
Herniation of the cerebellar tonsils
Hindbrain herniation
Kyphosis
Lordosis
Malformation
Malformation of lumbosacral
Malformation of spine
Malformation of the bladder
Platyspondylisis
Supernumerary vertebra
Unspecified or not associated with scoliosis
Vesical fistula
Vesical malformation

Vertaling van "vesical malformation " (Engels → Nederlands) :

malformation of the bladder | vesical malformation

misvorming van de blaas


Chiari I herniation | Chiari I malformation | Chiari malformation type I

Chiari type 1 malformatie


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

Chiari malformatie


dysgenesis | malformation

dysgenesie | gebrekkige ontwikkeling




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

mozaïektrisomie 9


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

congenitale | kyfose | niet-gespecificeerd of niet verband houdend met scoliose | congenitale | lordose | niet-gespecificeerd of niet verband houdend met scoliose | congenitale | misvorming van lumbosacraal (gewricht) gebied | niet-gespecificeerd of niet verband houdend met scoliose | congenitale | ontbreken van wervel | niet-gespecificeerd of niet verband houdend met scoliose | congenitale | vergroeiing van wervelkolom | niet-gespecificeerd of niet verband houdend met scoliose | extra wervelniet-gespecificeerd of niet verband houdend met scoliose | hemivertebraniet-gespecificeerd of niet verband houdend met scoliose | misvorming van wer ...[+++]


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

congenitale adrenale hyperplasie als gevolg van cytochroom P450-oxidoreductasedeficiëntie


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

branchio-otisch syndroom






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Date index: 2022-12-12
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