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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric radiology 9 (1980), S. 167-170 
    ISSN: 1432-1998
    Keywords: Osteosarcoma ; Pulmonary metastases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Five cases of osteosarcoma with rare clinical and/or radiographic findings are reported. A bony neoplasm should be suspected in each case with unexplained local or generalised sings and/or symptoms.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric radiology 2 (1974), S. 61-64 
    ISSN: 1432-1998
    Keywords: Dwarfism ; bone dysplasia ; spondylo-meta-epiphyseal dysplasia micromelic type
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A 4 8/12 years old girl with micromelic type of spondylo-meta-epiphyseal dysplasia is described. The spondylo-meta-epiphyseal dysplasias of micromelic type present a group of diseases with versatile clinical and radiographic findings. Marked shortening of stature with generalised spondylo-meta-epiphyseal changes in radiographic examination are a constant finding. No biochemical changes were yet reported. The difficulties of early recognition and classification of these cases are stressed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric radiology 1 (1973), S. 8-11 
    ISSN: 1432-1998
    Keywords: Death dwarfism ; thanatophoric dwarfism II ; bone dysplasia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A ‘new’ type of lethal bone osteochondrodysplasia — Thanatophoric Dwarfism II — is described. — Symmetrical shortening of both the trunk and extremities and coarse facial features are the most important morphologic findings. The fetuses are stillborn, premature, or die soon after the birth. In radiographic examination some shortening of the long and tubular bones with flaring, cupping and irregularity of the metaphyseal areas is present. The ischial and pubic bones are unossified but in contrast the iliac bones are fairly well developed and show triradiate acetabular roofs. The vertebral column in the lateral projection shows a wide ossification gap between the vertebral bodies and vertebral arches. Anterior shortening and flaring of the ribs is present. The ossification of the cranium and clavicles is grossly normal. Thanatophoric Dwarfism II is usually confused with Achondrogenesis as described by Parenti. Further diagnostic difficulties may arise with Thanatophoric Dwarfism of Maroteaux and Achondroplasia. — The authors point out that more types of lethal osteochondrodysplasias exist.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric radiology 10 (1980), S. 42-45 
    ISSN: 1432-1998
    Keywords: Rothmund-Thomson syndrome ; Osteosarcoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The first case of osteosarcoma in a 13 year old boy with Rothmund-Thomson syndrome is reported. The association between these two conditions in uncertain.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric radiology 10 (1980), S. 46-50 
    ISSN: 1432-1998
    Keywords: Dwarfism ; Skeletal dysplasia ; Metaphyseal dysplasia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A ten year old South African girl of mixed ancestry presented with gross facial abnormalities and dwarfism consequent upon a bizarre skeletal dysplasia. The main radiographic features were craniostenosis, fibrous dysplasia, metaphyseal lucencies and platyspondyly. Intelligence was normal and there were no systemic ramifications. The term “osteoglophonic dwarfism” is a succinct and apt designation for this remarkable disorder.
    Type of Medium: Electronic Resource
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