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Absence or aplasia of prostate
Congenital absence of the extensor pollicis longus
Congenital absence of the kidney
Congenital absence of the patella
Congenital absence of the vas deferens
Congenital absence of thumb extensors
Congenital clasped thumb
Congenital flexion-adduction deformity of thumb
Congenital hypoplasia of thumb extensors
Flex
Infant's persistent thumb-clutched hand
Patellar aplasia
Pollex varus
Spermatic cord
Thumb-clutched hand

Traduction de «Congenital absence the vas deferens » (Anglais → Français) :

Absence or aplasia of:prostate | spermatic cord | Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS

Absence ou aplasie de:cordon spermatique | prostate | Malformation congénitale du canal déférent, de l'épididyme, des vésicules séminales et de la prostate SAI


Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate

Autres malformations congénitales du canal déférent, de l'épididyme, des vésicules séminales et de la prostate


congenital absence of the vas deferens

absence congénitale du déférent


congenital clasped thumb [ congenital flexion-adduction deformity of thumb | pollex varus | congenital absence of thumb extensors | congenital hypoplasia of thumb extensors | infant's persistent thumb-clutched hand | thumb-clutched hand | congenital absence of the extensor pollicis longus | flex ]

pouce flexus-adductus congénital


patellar aplasia [ congenital absence of the patella ]

aplasie rotulienne [ apatellie | agénésie rotulienne | absence congénitale de rotule ]


This syndrome has characteristics of neonatal blisters, milia and congenital absence of dermatoglyphics on the hands and feet. It has been reported in two kindreds (one of which contained 13 affected individuals spanning three generations) and in an

syndrome de Baird




A very rare congenital malformation of the digits with the absence of the middle phalanges (usually of digits two to five), nail dysplasia and duplicated terminal phalanx of the thumb. Has been described in patients from two unrelated families.

brachydactylie type A5


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