| Literature DB >> 3591834 |
D Gossage, J M Perrin, M G Butler.
Abstract
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 congenital anomalies and associated findings are consistent with a diagnosis of the Marden-Walker syndrome. He also had mild pyloric stenosis and duodenal bands, not previously reported in this syndrome. This syndrome appears to be an autosomal recessive trait in some families. A summary of findings of the 16 previous published patients is presented.Entities:
Mesh:
Year: 1987 PMID: 3591834 PMCID: PMC5493387 DOI: 10.1002/ajmg.1320260420
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299