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Acrochondrohyperplasia
Acromacria
Amyoplasia
Amyoplasia congenita
Arachnodactily
Arthrogryposis multiplex congenita
Congenital amyoplasia
Congenital mesodermal dystrophy
Congenital multiple arthrogryposis
Congenital myotonia
Congenital preauricular fistula
Congenital retinal septum
Dolichostenomelia
Dystrophia mesodermalis congenita
Fistula auris congenita
Hyperchondroplasia
Marfan's abiotrophy
Marfan's dolichostenomely
Marfan's syndrome 1
Marfan-Achard syndrome
Myodystrophia fetalis
Myotonia congenita
Paramyotonia congenita
Spider fingers
Streblodactyly
Thomsen's disease

Vertaling van "Amyoplasia congenita " (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 ]






ablatio falciformis congenita retinae 2.ablatio falciformis congenita | congenital retinal septum

décollement falciforme congénital de la rétine


arachnodactily | Marfan's abiotrophy | Marfan's dolichostenomely | Marfan's syndrome 1 | Marfan-Achard syndrome | acrochondrohyperplasia | acromacria | congenital mesodermal dystrophy | dolichostenomelia | dystrophia mesodermalis congenita | hyperchondroplasia | spider fingers | streblodactyly

arachnodactylie | acromacrie | dolichosténomélie de Marfan | hyperchondroplasie | syndrome de Marfan


congenital preauricular fistula [ fistula auris congenita ]

fistule auriculaire congénitale [ coloboma auris | incisura auris ]


myotonia congenita [ Thomsen's disease | congenital myotonia ]

maladie de Thomsen [ myotonie congénitale ]


paramyotonia congenita

paramyotonie congénitale | maladie de von Eulenburg


An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to

syndrome d'aplasie cutanée congénitale-lymphangiectasie intestinale


A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c

leucémie aigüe myéloïde héréditaire


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