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Benign Samaritan congenital myopathy
Birth defect
CCHS
Congenital anomaly
Congenital auditory imperception
Congenital central alveolar hypoventilation
Congenital central hypoventilation syndrome
Congenital deafness
Congenital defect
Congenital deformity
Congenital disease
Congenital disorder
Congenital malformation
Congenital muscular dystrophy NOS
Congenital myopathies
Disease central core
Hypoparathyroidism
Idiopathic central alveolar hypoventilation
Minicore
Multicore
Myopathy in hyperparathyroidism
Nemaline
Ondine syndrome
Ondine's Curse
Sleep-induced apnea
Thyrotoxic myopathy

Vertaling van "congenital myopathies " (Engels → Nederlands) :



A rare genetic, non-dystrophic myopathy with characteristics of fatigable muscle weakness associated with congenital myopathy. Patients present with axial hypotonia, myopathic facies with fatigable ptosis, feeding difficulties, delayed gross motor de

congenitale myopathie met myasthenie-achtige aanvang


Benign Samaritan congenital myopathy

goedaardige Samaritaanse congenitale myopathie


A rare genetic lethal non-dystrophic congenital myopathy disorder characterized, antenatally, by fetal akinesia, intrauterine growth restriction and polyhydramnios, and, following birth, by severe neonatal hypotonia, severe generalized skeletal, bulb

congenitale letale myopathie, Compton-North-type


birth defect | congenital anomaly | congenital defect | congenital disease | congenital disorder | congenital malformation

aangeboren aandoening


congenital disease [ congenital deformity | congenital malformation ]

aangeboren ziekte [ aangeboren afwijking ]


Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline

central-core-disease | congenitale spierdystrofie | NNO | congenitale spierdystrofie | met specifieke morfologische-afwijkingen van spiervezel | fibre-type disproportion | minicore disease | multicore disease | myopathie | myotubulair (centronucleair) | myopathie | nemaline lichaampjes


congenital auditory imperception | congenital deafness

congenitale doofheid


congenital central alveolar hypoventilation | congenital central hypoventilation syndrome | idiopathic central alveolar hypoventilation | Ondine syndrome | Ondine's Curse | sleep-induced apnea | CCHS [Abbr.]

congenitaal centraal hypoventilatie-syndroom


Myopathy in:hyperparathyroidism (E21.0-E21.3+) | hypoparathyroidism (E20.-+) | Thyrotoxic myopathy (E05.-+)

myopathie bij | hyperparathyroïdie (E21.0-E21.3) | myopathie bij | hypoparathyroïdie (E20.-) | thyrotoxische myopathie (E05.-)


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