Identical twins with Weissenbacher-Zweymuller syndrome and neural tube defect

J. C. Ramer, K. Eggli, P. K. Rogan, R. L. Ladda

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Abstract

Neurologic abnormalities have been described only once previously in a child with Weissenbacher-Zweymuller syndrome (WZS), a rare skeletal dysplasia, evident neonatally. We report on identical twin male infants with skeletal findings typical of WZS, including small size at birth, proximal limb shortness, mid face hypoplasia, and myopia. In addition, twin B had a parieto occipital encephalocele while twin A had a meningocele at the same location. Twin B has had significant delays in development and hearing loss.

Original languageEnglish (US)
Pages (from-to)614-618
Number of pages5
JournalAmerican Journal of Medical Genetics
Volume45
Issue number5
DOIs
StatePublished - Jan 1 1993

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All Science Journal Classification (ASJC) codes

  • Genetics(clinical)

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