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Am J Med Genet ; 35(3): 443-6, 1990 Mar.
Article in English | MEDLINE | ID: mdl-2309796

ABSTRACT

Acrocallosal syndrome is an autosomal recessive disorder of brain malformation and complex polydactyly. We report on an additional patient with this disorder. It is suggested that increased birth weight and cerebellar hypoplasia occur in acrocallosal syndrome. The finding of an extra bone within the anterior fontanel in our patient suggests similarity to the Xt mouse mutant, which is homologous to Greig syndrome in man. This provides additional support for the hypothesis of allelism of the Greig and acrocallosal syndromes.


Subject(s)
Brain/abnormalities , Foot Deformities/genetics , Genes, Recessive , Animals , Brain/diagnostic imaging , Foot Deformities/diagnostic imaging , Humans , Infant, Newborn , Male , Mice , Radiography , Syndrome
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