"Duplicate calcaneus": A rare developmental defect observed in several skeletal dysplasias

Pediatric Radiology

Volumn 31, Issue 1, 2001, Pages 38-42

  Cormier Daire, V ^a   Savarirayan, R ^a   Unger, S ^a   Rimoin, D L ^a   Lachman, R S ^a  

^a CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BONE DYSPLASIA; CALCANEUS DUPLICATION; CHILD; CHONDRODYSPLASIA; CHONDRODYSPLASIA PUNCTATA; DATA ANALYSIS; DATA BASE; DEVELOPMENTAL DISORDER; FETUS; FOOT RADIOGRAPHY; HUMAN; INFANT; MAJOR CLINICAL STUDY; OSSIFICATION; PRIORITY JOURNAL; REGISTER; THANATOPHORIC DWARFISM;

BONE DISEASES, DEVELOPMENTAL; CALCANEUS; CHILD; HUMANS; REGISTRIES;

EID: 0035141430     PISSN: 03010449     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002470000354     Document Type: Article

References (10)

1. Molecular, radiological and histopathological correlations in Thanatophoric dysplasia
2. International nomenclature and classification of the osteochondrodysplasias
3. Larsen's syndrome
4. Atelosteogenesis type III. Long term survival, prenatal diagnosis and evidence for dominant transmission
5. Anomalous multifocal ossification of the os calcis
6. An autosomal dominant syndrome of short stature with mesomelic shortness of limbs, abnormal carpal and tarsal bones, hypoplastic middle phalanges, and bipartite calcunei
7. Clinical report: Autopsy findings in a stillborn infant with the Osebold-Remondini syndrome
8. Osebold-Remondini syndrome vs chondrodysplasia punctata
9. Punctate epiphyses: A radiological sign not a disease
10. Chondrodysplasia punctata and maternal systemic lupus erythematosous