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Aarskog
Blount
Cockayne
De Lange
Dubowitz
Holt-Oram
Klippel-Trenaunay-Weber
Morbus Blount
Nagel-patella
Noonan
Osgood-Schlatter
Osteochondrose
Osteochondrosis deformans tibiae
Prader-Willi
Proximale tibia
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Bernard
Syndroom van Blount
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Horner
Syndroom van Horner-Bernard
TAR-syndroom
Tibia vara
Trombocytopenie met ontbreken van radius
Tuberositas tibiae
VATER-syndroom
Ziektebeeld

Traduction de «syndroom van blount » (Néerlandais → Anglais) :

osteochondrosis deformans tibiae | syndroom van Blount | tibia vara

Blount disease | Blount syndrome | Blount-Barber disease | Blount-Barber syndrome




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




osteochondrose (juveniel) van | proximale tibia [Blount] | osteochondrose (juveniel) van | tuberositas tibiae [Osgood-Schlatter] | tibia vara

Osteochondrosis (juvenile) of:proximal tibia [Blount] | tibial tubercle [Osgood-Schlatter] | Tibia vara


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


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

Pseudohypoparathyroidism type Ia


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




datacenter (28): www.wordscope.be (v4.0.br)

'syndroom van blount' ->

Date index: 2022-07-23
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