Vertaling van "Congenital multiple arthrogryposis " (Engels → Frans) :

arthrogryposis multiplex congenita [ amyoplasia congenita | myodystrophia fetalis | congenital multiple arthrogryposis ]
arthrogrypose congénitale multiple [ amyoplasie congénitale | arthrogryposis multiplex congénitale | raideur articulaire congénitale | arthrogrypose | myodystrophie foetale ]

Congenital multiple pituitary hormone deficiency including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Rare when compared with t
déficits hypohysaires multiples de cause génétique identifée

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
syndrome de McDonough

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
syndrome de Verloove-Van Horick-Brubakk

Congenital:anomaly | deformity | disease or lesion | multiple anomalies | NOS of brain
Anomalie congénitale | Anomalies multiples congénitales | Maladie ou lésion congénitale | SAI de l'encéphale

Multiple congenital exostoses
Exostoses multiples congénitales

Congenital malformation of renal artery NOS Multiple renal arteries
Artères rénales multiples Malformation congénitale de l'artère rénale SAI