Traduction de «Congenital myopathies » (Anglais → Néerlandais) :

Congenital myopathies
congenitale myopathieën

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.-)