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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of gynecology and obstetrics 233 (1983), S. 141-147 
    ISSN: 1432-0711
    Keywords: Chromosomal mosaicism ; Turner's syndrome ; Gonadal dysgenesis ; Dysgerminoma ; Gonadoblastoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We report a 16-year-old girl with features of Turner's syndrome from whom an invasive dysgerminoma was removed. Cytotoxic drugs were given for the next 12 months. Mosaicism of two karyotypes (45,X/46,X; mar) was found in various tissues. The literature is reviewed with special regard to cytogenetic findings and prognosis of malignant growth and differentiation of dysgenetic gonads.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 102 (1968), S. 49-61 
    ISSN: 1432-1076
    Keywords: Chromosomenaberrationen ; Multiple Mißbildungen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Bericht über zwei neue Beobachtungen einer autoradiographisch gesicherten Deletion der kurzen Arme eines Chromosoms B4. Das dadurch verursachte Mißbildungssyndrom zeichnet sich durch eine kraniofaciale Dysmorphie mit Mikrocephalie, Hypertelorismus, kräftiger, nach unten gebogener Nase und Mikroretrogenie aus. Dysrhaphische Störungen sind als Gaumenspalte, Iriscolobom und Hirnmißbildungen (interventriculäre Cyste; cavum septi pellucidi) ausgeprägt. Bei Knaben besteht eine Hypospadie. Die Papillarleistenmuster sind in großen Bezirken aufgelöst.
    Notes: Summary Two new cases of a deletion of the short arm of one chromosome B 4 are reported. This aberration causes a syndrome of congenital malformations which is characterized by cranio-facial dysmorphia (microcephaly, hypertelorism, beaked nose, micrognathia), midline fusion defects (cleft palate, coloboma of the iris), cerebral abnormality (interventricular cyst; cavum septi pellucidi), hypospadias in males and decomposition of dermatoglyphics in large areas.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 116 (1973), S. 1-12 
    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
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