Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome.
H Santos, J Mateus, MJ Leal - Journal of medical genetics, 1988 - jmg.bmj.com
H Santos, J Mateus, MJ Leal
Journal of medical genetics, 1988•jmg.bmj.comAn association of Hirschsprung disease with polydactyly, unilateral renal agenesis,
hypertelorism, and congenital deafness is described in sibs (brother and sister) of
consanguineous parents. It is suggested that this might represent a new autosomal
recessive syndrome.
hypertelorism, and congenital deafness is described in sibs (brother and sister) of
consanguineous parents. It is suggested that this might represent a new autosomal
recessive syndrome.
An association of Hirschsprung disease with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness is described in sibs (brother and sister) of consanguineous parents. It is suggested that this might represent a new autosomal recessive syndrome.
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