Abstract
We describe a girl who presents the features of Wiedemann-Rautenstrauch syndrome. This autosomal recessive condition has characteristic radiographic findings which can be considered manifestations of the syndrome.
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References
Rautenstrauch T, Snigula F, Krieg T, Gay S, Müller PK (1977) Progeria: a cell culture study and clinical report of familial incidence. Eur J Pediatr 124: 101
Wiedemann HR (1979) An unidentified neonatal progeroid syndrome: follow-up report. Eur J Pediatr 130: 65
Devos EA, Leroy JG, Frijns JP, Van den Berghe H (1981) The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Eur J Pediatr 136: 245
Ohashi H, Eguchi T, Kajii T (1987) Neonatal progeroid syndrome: report of a Japanese infant. Jpn J Hum Genet 32: 253
Rudin C, Thommen L, Fliegel C, Steinmann B, Bühler U (1988) The neonatal pseudo-hydrocephalic progeroid syndrome (Wiedemann-Rautenstrauch). Report of a new patient and review of the literature. Eur J Pediatr 147: 433
Hagadorn JI, Wilson WG, Hogge WA, Callicott JH, Beale EF (1990) Neonatal progeroid syndrome: more than one disease? Am J Med Genet 35: 91
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Obregon, M.G., Bergami, G.L., Giannotti, A. et al. Radiographic findings in Wiedemann-Rautenstrauch syndrome. Pediatr Radiol 22, 474–475 (1992). https://doi.org/10.1007/BF02013521
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DOI: https://doi.org/10.1007/BF02013521