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Cumming syndrome with heterotaxia, campomelia and absent uterus/fallopian tubes

✍ Scribed by M.F. Bedeschi; L. Spaccini; T. Rizzuti; D.A. Coviello; P. Castorina; F. Natacci; F. Lalatta


Book ID
101446918
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
34 KB
Volume
132A
Category
Article
ISSN
1552-4825

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Heterotaxia in a fetus with campomelia,
✍ Ming, Jeffrey E.; McDonald-McGinn, Donna M.; Markowitz, Richard I.; Ruchelli, Ed πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 42 KB πŸ‘ 2 views

We report on a fetus with tetramelic campomelia, polysplenia, multicystic dysplastic kidneys, and cervical lymphocele. This condition is similar to the autosomal recessive condition described by Cumming et al. [1986: Am J Med Genet 25:783-790] and is different from campomelic syndrome. In addition,