Abstract
A 3-month-old male child presented with typical features of acrocallosal syndrome. He satisfies Courten’s diagnostic criteria for acrocallosal syndrome
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Koenig R, Bach A, Woelki U, Grzeschik KH, Fuchs S. Spectrum of the acrocallosal syndrome.Am J Med Genet 2002; 108: 7–11.
Christianson AL, Venter PA, Du Toit JL, Shipalana N, Gericke GS. acrocallosal syndrome in two African brothers born to consanguineous parents.Am J Med Genet 1994; 51:98–101.
Casamassima AC, Beneck D, Gewitz MHet al. Acrocallosal syndrome: Additional manifestations.Am J Med Genet 1989; 32: 311–317.
Moeschler JB, Pober BR, Homes LB, Graham JM. Acrocallosal syndrome: new findings.Am J Med Genet 1989; 32:306–310.
Turrolla L, Dementi M, Tenconi R. How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case.J Med Genet 1990; 27: 516–518.
Courtens W, Vamos E, Christophe C, Schinzel A. Acrocallosal syndrome in an Algerian boy born to consanguineous parents: review of the literature and further delineation of the syndrome.Am J Med Genet 1997; 69:17–22.
Rauch A, Trautmann U, Pfeiffer RA. Clinical and molecualr cytogenetic observations in three cases of “Trisomy 12p syndrome”.Am J Med Genet 1996; 63:243–249.
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Gupta, A., Thakur, S. & Phadke, S.R. Diagnosing acrocallosal syndrome. Indian J Pediatr 70, 177–179 (2003). https://doi.org/10.1007/BF02723750
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DOI: https://doi.org/10.1007/BF02723750