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Brief Clinical Report and Review: A 26-Month-Old Child With Marden-Walker Syndrome and Pyloric Stenosis
We recently examined a 26-month-old boy with abnormal face, blepharophimosis, hypertelorism, apparently low-set ears, micrognathia, arachnodactyly, talipes equinovarus, and joint contractures. Subsequently he manifested failure to thrive, respiratory infections, and developmental delay. These congen...
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| Gepubliceerd in: | Am J Med Genet |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
1987
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5493387/ https://ncbi.nlm.nih.gov/pubmed/3591834 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.1320260420 |
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