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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 129 (1978), S. 215-218 
    ISSN: 1432-1076
    Keywords: Osteogenesis imperfecta tarda ; Osteogenic sarcoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We describe the case history of a 13 years old boy who developed osteogenic sarcoma of the left thigh, six years after diagnosis of osteogenesis imperfecta tarda with a positive family history. Only four other patients with this disease combination are reported in the literature. Preoperative treatment with high-dose Methotrexate caused marked tumor regression, as shown at examination of amputation material. The inter-relationships between the two disorders are discussed and the literature is briefly reviewed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1076
    Keywords: Hemihypertrophy ; Malignant giant pheochromocytoma ; Neuroectodermal dysplasia syndromes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This is apparently the first report on connatal hemihypertrophy with malignant pheochromocytoma. The coincidence of hemihypertrophy with other diseases, particularly neuroectodermal dysplasias on the one hand and the frequent association of neuroectodermal dysplasias with pheochromocytoma on the other, are emphasized. Furthermore, basically known particularities of this case as malignancy of the tumor, the unusual size of the tumor in children, and the normal catecholamine levels in serum as well as the normal excretion of vanillylmandelic acid are discussed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 132 (1979), S. 131-132 
    ISSN: 1432-1076
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 130 (1979), S. 65-70 
    ISSN: 1432-1076
    Keywords: Progeroid ; Pseudohydrocephalus ; Natal teeth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Two male infants with a pseudo-hydrocephalic progeroid syndrome with natal teeth are compared with two very similar female cases reported in the literature and interpreted as congenital progeria. All these cases may represent a separate entity, a previously unrecognized genetic progeroid syndrome.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1076
    Keywords: Focal dermal hypoplasia ; Goltz-Gorlin Syndrome ; Diaphragmatic hernia ; Asymmetric malformations ; Dominant X-linked inheritance with lethality in male fetuses
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We report a female newborn with focal dermal hypoplasia (Goltz-Gorlin Syndrome) and marked asymmetric malformations on the right side of the body. Diaphragmatic hernia on the same side, which has not been reported in this syndrome, led to perinatal complications.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 128 (1978), S. 65-65 
    ISSN: 1432-1076
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 129 (1978), S. 99-101 
    ISSN: 1432-1076
    Keywords: Lipidoses ; Niemann-Pick disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Autopsy material from a case of Niemann-Pick disease was subjected to lipid analysis. Among the six tissues investigated, lymph nodes exhibited the greatest storage of several lipids. Since lymph nodes are relatively easy to obtain by biopsy, they may be utilized for chemical diagnosis of this type of lipidosis.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 43 (1978), S. 245-245 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 26 (1975), S. 271-289 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Zusammenfassung Wir berichten über ein 5 1/2jähriges Mädchen, deren klinische Symptomatik die Diagnose eines Cat eye-Syndroms gestattet. Die führenden Leitsymptome sind: Analstenose, präauriculäre Anhängsel und Fisteln, iridale Kolobome, gedoppelte Ureterbecken mit Ureterfissus beidseits, vesico-urethraler Reflux rechts und normale geistige Entwicklung. Alkalische Leukocytenphosphatase im Normbereich. Die Chromosomenanalyse zeigte bei sonst unauffäulligem Karyotyp ein überzähliges submetazentrisches Chromosom, das von der Größe her kleiner als die Chromosomen der G-Gruppe war und Satelliten auf dem kurzen und langen Arm aufwies. Autoradiographische Untersuchungen zeigten eine späte DNS-Replikation dieses Chromosoms. Die Giemsa-Banden-Technik führte zur intensiven Bänderung der Chromatiden mit ungefärbten Satellitenregionen. Mit der Fluorescenzfärbung ließ sich eine intensive punktförmige Fluorescenz der Satellitenregionen nachweisen. Die heterochromatischen Chromatiden zeigten eine homogene Fluorescenz. Auch die C-Banden-Technik führte zur homogenen Anfärbung der Chromatiden unter Ausschluß der Satellitenregionen. Dagegen führte die Giemsa-11-Technik zur deutlichen Kontinuitätsunterbrechung heterochromatischen Materials zwischen Zentromerregion und dem distalen langen Arm. Ebenfalls blieben hier die Satellitenregionen ungefärbt. Trotz Anwendung aller modernen cytogenetischen Untersuchungsmethoden gelang es nicht, die Herkunft dieses überzähligen Marker-Chromosoms zu identifizieren.
    Notes: Summary We report a 5 1/2-year-old girl whose clinical symptoms are consistent with diagnosis of the cat-eye syndrome. The prominent symptoms are: anal stenosis, preauricular tags and pits, coloboma of the iris, doubling of the pelvis and ureter on both sides, vesicourethral reflux on the right side and normal mental development. Leucocyte alkaline phosphatase is normal. Chromosomal analysis shows a supernumerary submetacentric chromosome. This extra chromosome is smaller than the G-group chromosomes and has satellites on the short and long arms. Autoradiography after 3H-thymidine incorporation shows a late-labeling marker chromosome. After using the Giemsa-banding technique, the chromatids demonstrate dark bandings with only soft, unstained satellites. With the fluorescence method, one can see spotlike fluorescence of the satellites on both arms and diffuse fluorescence of the heterochromatic segments. In addition, the C-bandings demonstrate a homogeneous dark staining of the chromatids, but we not find stained satellites. Using the Giemsa-11 technique one can see the 47th chromosome with predominantly heterochromatic parts, but small euchromatic segments are visible between them. Satellites are unstained. Using currently accepted cytogenetical methods, it is not possible to identify the origin of this supernumerary marker chromosome.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 28 (1975), S. 353-356 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Zusammenfassung Ein Fall von Tetraphokomelie und Oberkieferspalte wird beschrieben. Die Ähnlichkeit dieses Patienten mit Fällen, die als Pseudothalidomid-oder Robert-Syndrom eingeordnet werden, läßt die Frage aufkommen, ob eine Unterscheidung dieser beiden Syndrome sinnvoll ist.
    Notes: Summary A new case of Tetraphocomelia—cleft palate syndrome is described. The similiarity between this patient and the cases classified as Pseudothalidomide or as Robert syndrome makes a distinction between these 2 syndromes doubtful.
    Type of Medium: Electronic Resource
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