Miller syndrome (postaxial acrofacial dysostosis): further evidence for autosomal recessive inheritance and expansion of the phenotype.
case_report · Level V
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- Record sourced from PubMed, PMID 1941965.
- Also identified by PMC identifier 1017057.
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Abstract
A sibship with postaxial acrofacial dysostosis syndrome (Miller syndrome) is reported. In addition to the characteristic facial and limb defects, previously undescribed anomalies, including midgut malrotation, gastric volvulus, and renal anomalies, are recorded.
Medical subject headings
- Mandibulofacial Dysostosis