Abstract
ULLRICH-TURNER syndrome comprises stunted stature, poorly developed secondary sexual characteristics, a typical facies and variable cardiac malformations. Affected persons, who are all female, have an aberrant or absent X-chromosome.
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References
Ford CE, Jones KW, Polani PE, de Almeida JC, Briggs JH (1959) A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner’s Syndrome). Lancet I: 711
Opitz JM (1991) Editorial Comment. Otto Ullrich: An appreciation. Am J Med Genet 41:126–127
Seresevskij NA (1925) In relation to the question of a connection between congenital abnormalities and endocrinopathies. The Russian Endocrinological Society on 12th November Turner HH (1938) A syndrome of infantilism, congenital webbed neck and cubitus valgus. Endocrinology 23: 566–574
Ullrich O (1930) Über typische Kombinationsbilder multipler Abartungen. Z Kinderheilk 49: 271–276
Ullrich O (1949) Turner’s syndrome and status Bonnevie-Ullrich. Am J Hum Genet 1:179–202
Wiedemann H-R (1991) Otto Ullrich and His Syndromes. Am J Med Genet 41: 128–133
Wiedemann H-R, Glazl CJ (1991) Follow-up of Ullrich’s original patient with “Ullrich-Turner” syndrome. Am J Med Genet 41:134–136
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© 1997 Springer-Verlag London Limited
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Beighton, P., Beighton, G. (1997). ULLRICH, Otto. In: The Person Behind the Syndrome. Springer, London. https://doi.org/10.1007/978-1-4471-0925-9_84
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DOI: https://doi.org/10.1007/978-1-4471-0925-9_84
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