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Digitale Medien

The acrocallosal syndrome (1988)

Philip, N. ; Apicella, N. ; Lassman, I. ; [weitere]

Springer

European journal of pediatrics 147 (1988), S. 206-208

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Details

ISSN: 1432-1076

Schlagwort(e): Acrocallosal syndrome ; Recessive mode of inheritance ; Greig syndrome

Quelle: Springer Online Journal Archives 1860-2000

Thema: Medizin

Notizen: Abstract The acrocallosal syndrome is characterized by peculiar facies, polydactyly of the hands and/or feet, and agenesis of the corpus callosum. Two unrelated 4-month-old boys with consanguineous parents are reported. Both exhibited the main features of the syndrome, but neither of them had partial reduplication of halluces. Consequently, pre-axial polydactyly of the feet is not considered to be a constant feature of the acrocallosal syndrome. The similarity of the acrocallosal syndrome to Greig syndrome is discussed, but it appears unlikely that the two syndromes are identical. Consanguinity in both cases is a strong argument in favour of a recessive mode of inheritance.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1007/BF00442226

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