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Spondylometaphyseal dysplasia, Czarny-Ratajczak type

MedGen UID:
1681091
Concept ID:
C5190628
Disease or Syndrome
Synonyms: Spondylometaphyseal dysplasia Czarny Ratajczak type; spondylometaphyseal dysplasia, Czarny-Ratajczak type
SNOMED CT: Spondylometaphyseal dysplasia Czarny Ratajczak type (782820003)
 
Monarch Initiative: MONDO:0018255
Orphanet: ORPHA370019

Definition

A rare primary bone dysplasia disorder characterised by short stature with severe shortening of limbs, genu vara deformity and enlarged joints with movement limitation particularly affecting the hip joints. Radiological findings show coxa vara, generalised metaphyseal irregularities of the tubular bones (including cupping, fraying and splaying), which are more severe in the femur and forearm bones than the metacarpals and phalanges and vertebral abnormalities including ovoid vertebral bodies with anterior rectangular protrusions and severe platyspondyly. [from SNOMEDCT_US]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVSpondylometaphyseal dysplasia, Czarny-Ratajczak type

Recent clinical studies

Diagnosis

Bieganski T, Beighton P, Lukaszewski M, Bik K, Kuszel L, Wasilewska E, Kozlowski K, Czarny-Ratajczak M
Eur J Med Genet 2017 Oct;60(10):509-516. Epub 2017 Jul 4 doi: 10.1016/j.ejmg.2017.07.004. PMID: 28687525Free PMC Article
Czarny-Ratajczak M, Chrzanowska K, Bieganski T, Sulko J, Baranska D, Kocyla-Karczmarewicz B, Kuszel L, Jakubowski L, Niedzielski K, Kozlowski K
Am J Med Genet A 2009 Oct;149A(10):2166-72. doi: 10.1002/ajmg.a.33016. PMID: 19764033

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