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Abscess
Aran-Duchenne disease
Atrophy
Atrophy of salivary gland
Bulbourethral gland
Cowper's gland
Cowperian glands
Cruveilhier disease
Dacryops Dry eye syndrome Lacrimal cyst
Gland atrophy
Infantile spinal muscular atrophy
Littré's gland
PMA
Periurethral
Progressive muscular atrophy
Progressive muscular atrophy of infancy
Progressive spinal muscular atrophy
SMA
SMA I
SPMA
Severe infantile spinal muscular atrophy
Spinal muscular atrophy
Spinal muscular atrophy type I
Spinal progressive muscular atrophy
Urethral
Wasting
Werdnig-Hoffman disease

Vertaling van "Gland atrophy " (Engels → Nederlands) :

Dacryops Dry eye syndrome Lacrimal:cyst | gland atrophy

dacryops | droge-ogensyndroom | traanklieratrofie | traankliercyste


infantile spinal muscular atrophy | progressive muscular atrophy of infancy | severe infantile spinal muscular atrophy | spinal muscular atrophy type I | Werdnig-Hoffman disease | SMA I [Abbr.]

infantiele spinale spieratrofie | Spinale musculaire atrofie type I | ziekte van Werdnig-Hoffmann | SMA type I [Abbr.]


Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]

spieratrofie van Aran-Duchenne | ziekte van Duchenne-Aran




bulbourethral gland | Cowperian glands | Cowper's gland

glandulae bulbocavernosae | glandulae bulbourethrales | glandulae cowperi | klieren van Cowper


Abscess (of):Cowper's gland | Littré's gland | periurethral | urethral (gland)

abces (van) | klier van Littré | abces (van) | klieren van Cowper | abces (van) | periurethraal | abces (van) | urethra(klier)


A rare endocrine disease with characteristics of the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy

Wolfram-achtig syndroom


A rare hereditary motor and sensory neuropathy disorder with characteristics of the typical CMT phenotype (slowly progressive distal muscle atrophy and weakness in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tend

autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type F


A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hyp

X-gebonden myopathie met posturale spieratrofie


atrophy | wasting

atrofie | verschrompeling van organen


w