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  • 1
    Electronic Resource
    Electronic Resource
    A new familial skeletal dysplasia with severely retarded ossification and abnormal modeling of bones especially of the epiphyses, the hands, and feet (1984)
    Springer
    European journal of pediatrics 141 (1984), S. 231-235 
    Details
    ISSN: 1432-1076
    Keywords: New skeletal dysplasia ; Multiple epiphyseal dysplasia ; Delayed maturation of hand feet pelvis sacrum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Three brothers with a constitutional skeletal dysplasia characterized by an excessively retarded ossification, principally of the epiphyses, the pelvis, the hands and the feet, are reported. In the hands and feet the retarded ossification is combined with an abnormal modeling of the bones. All the children appeared normal at birth. At the time of examination a moderate degree of dwarfism could be predicted. There was no mental retardation. All laboratory investigations including chromosomal analyses and examination for acid mucopolysaccharides in the urine were normal. Parental consanguinity suggest an autosomal recessive inheritance. There is no resemblance of this disorder to any of the hitherto described groups of constitutional diseases of bones.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00572767
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Osteomalacia of the mother —rickets of the newborn (1987)
    Springer
    European journal of pediatrics 146 (1987), S. 292-293 
    Details
    ISSN: 1432-1076
    Keywords: Osteomalacia ; Neonatal rickets ; 25-hydroxy-vitamin D
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract During the last 4 years we observed four cases of neonatal rickets. The mothers of the infants suffered from osteomalacia for 1–3 years prior to its diagnosis shortly after the birth of their children. All four infants were born with craniotabes, and one infant had, in addition, a radial fracture. The diagnoses were confirmed by radiological and laboratory tests which revealed a rarefied bone structure, decreased serum 25-hydroxy-vitamin D and increased alkaline phosphatase levels in all patients. The disorder regressed under low-dose vitamin D3 therapy. As osteomalacia seems to be predominant in oriental women living in Berlin, it is necessary to consider vitamin D deficiency when clinical symptoms of this disease arise and to treat these women at least during pregnancy.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00716477
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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