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Case Reports
. 1992 Nov;29(11):831-3.
doi: 10.1136/jmg.29.11.831.

Lethal skeletal dysplasia owing to double heterozygosity for achondroplasia and spondyloepiphyseal dysplasia congenita

I D Young  1 , N R Ruggins, J M Somers, J M Zuccollo, N Rutter
Affiliations
Case Reports

Lethal skeletal dysplasia owing to double heterozygosity for achondroplasia and spondyloepiphyseal dysplasia congenita

I D Young et al. J Med Genet. 1992 Nov.

Abstract

A male infant with lethal short limbed dwarfism is described. His father had spondyloepiphyseal dysplasia congenita and his mother had achondroplasia. It is believed that the infant inherited both of these disorders and that their combined effects resulted in early death owing primarily to severe pulmonary hypoplasia.

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References

    1. Clin Genet. 1977 Jan;11(1):31-8 - PubMed
    1. Clin Endocrinol (Oxf). 1991 Apr;34(4):265-74 - PubMed
    1. Am J Hum Genet. 1989 Jul;45(1):5-15 - PubMed
    1. Am J Med Genet. 1988 Apr;29(4):955-61 - PubMed
    1. J Bone Joint Surg Br. 1982;64(4):435-41 - PubMed

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