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  • 1970-1974  (2)
  • Catch-up growth  (1)
  • Intra-uterine Growth Retardation  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Studies of malformation syndromes of man XXIV B: The Dubowitz syndrome. Further observations (1973)
    Springer
    European journal of pediatrics 116 (1973), S. 1-12 
    Details
    ISSN: 1432-1076
    Keywords: Recessive inheritance ; Parental consanguinity ; Mild mental retardation/normal intelligence ; Intrauterine growth retardation/shortness of stature/normal height ; Catch-up growth ; Microcephaly ; Malformation syndrome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This paper reports observations on 6 new patients with the Dubowitz syndrome which was first defined by Grosse et al., in 1971 and which is a recessively inherited, pleiotropic malformation syndrome including variable degrees of intrauterine growth retardation and primordial shortness of stature, microcephaly, mental retardation, eczema, and a characteristic appearance, voice and combination of minor anomalies. Data in the present report show that eczema can be absent, and patients can be of normal height, and of normal intelligence in spite of a head circumference which has so far always fallen below the third percentile. So far 11 patients (8 females and 3 males) are known with the Dubowitz syndrome; in one family the parents were first cousins.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00438824
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    The Dubowitz syndrome (1971)
    Springer
    European journal of pediatrics 110 (1971), S. 175-187 
    Details
    ISSN: 1432-1076
    Keywords: Intra-uterine Growth Retardation ; Shortness of Stature ; Microcephaly ; Mental Retardation ; Eczema ; Malformation Syndrome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung 4 Patienten mit einem bisher unbekannten Symptomenkomplex werden beschrieben. Die Hauptmanifestationen dieses Syndromes sind primärer Zwergwuchs, schwere Mikrocephalie mit erstaunlich leichter Beeinträchtigung der intellektuellen Fähigkeiten und eine charakteristische Physiognomie. 2 unserer Patienten sind Geschwister. Die Schwester eines 1965 von Dubowitz publizierten—und in diese Arbeit einbezogenen—Falles war wahrscheinlich betroffen. Sie starb im Alter von 3 Monaten. Die Eltern aller Kinder sind normal. Wir nehmen an, daß dieses Syndrom recessiv vererbt wird.
    Notes: Abstract This paper reports observations on 4 patients with a newly recognized syndrome called the Dubowitz syndrome. Dubowitz provided some follow-up data on the patient he first described in 1965; in addition 3 personally studied patients are presented. To date the known patients have manifested intrauterine growth retardation (with primordial shortness of stature), microcephaly, variable degrees of eczema and mental retardation, and a characteristic facial appearance. It is presumed that the Dubowitz syndrome is recessively inherited.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00440382
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
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