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Aarskog
Acetabulum
Buchanan
Cockayne
Crista iliaca
De Lange
Dubowitz
Holt-Oram
Klippel-Trenaunay-Weber
Nagel-patella
Noonan
Osteochondrose
Pierson
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Symphysis pubica
Synchondrosis ischiopubica
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Adams
Syndroom van Adams-Stokes
Syndroom van Bernard
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Horner
Syndroom van Horner-Bernard
Syndroom van Morgagni
Syndroom van Pierson
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Van Neck
Ziekte van Adams-Stokes
Ziektebeeld

Traduction de «Syndroom van Pierson » (Néerlandais → Anglais) :

syndroom van Pierson

Rare syndrome with the association of congenital nephrotic syndrome, ocular anomalies and microcoria. The disorder results in proteinuria with nephrotic syndrome and histological lesions marked by diffuse mesangial sclerosis. Ocular anomalies are pre




syndroom van Bernard | syndroom van Horner | syndroom van Horner-Bernard

Bernard-Horner syndrome


syndroom van Abderhalden-Fanconi | syndroom van Debré-de Toni-Fanconi | syndroom van Debré-Fanconi

A.-F.syndrome | cystine storage disease


syndroom van Adams | syndroom van Adams-Stokes | syndroom van Morgagni | ziekte van Adams-Stokes

Adams-Stokes disease | Adams-Stokes syndrome | Spens syndrome


osteochondrose (juveniel) van | acetabulum | osteochondrose (juveniel) van | crista iliaca [Buchanan] | osteochondrose (juveniel) van | symphysis pubica [Pierson] | osteochondrose (juveniel) van | synchondrosis ischiopubica [van Neck]

Osteochondrosis (juvenile) of:acetabulum | iliac crest [Buchanan] | ischiopubic synchondrosis [van Neck] | symphisis pubis [Pierson] |


syndroom van | Aarskog | syndroom van | Cockayne | syndroom van | de Lange | syndroom van | Dubowitz | syndroom van | Noonan | syndroom van | Prader-Willi | syndroom van | Robinow-Silverman-Smith | syndroom van | Russell-Silver | syndroom van | Seckel | syndroom van | Smith-Lemli-Opitz

Syndrome:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz


syndroom (van) | Holt-Oram | syndroom (van) | Klippel-Trenaunay-Weber | syndroom (van) | nagel-patella | syndroom (van) | Rubinstein-Taybi | syndroom (van) | sirenomelie | TAR-syndroom [trombocytopenie met ontbreken van radius] | VATER-syndroom

Syndrome:Holt-Oram | Klippel-Trénaunay-Weber | nail patella | Rubinstein-Taybi | sirenomelia | thrombocytopenia with absent radius [TAR] | VATER


SOLAMEN (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom

A rare genetic, poly malformative syndrome with characteristics of progressive, proportionate, asymmetric segmental overgrowth (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous


AHO-PHP (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia

Pseudohypoparathyroidism type Ia




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Date index: 2020-12-30
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