Citation, DOI, disclosures and article data
Citation:
Jones J, Baba Y, Glick Y, et al. Metaphyseal dysplasia. Reference article, Radiopaedia.org (Accessed on 26 Mar 2025) https://doi.org/10.53347/rID-16907
Metaphyseal dysplasia (also known as Pyle disease, metaphyseal chondrodysplasia, metaphyseal dysostosis) is a rare autosomal recessive disorder characterised by flaring of the ends of long bones with relative constriction and sclerosis of the diaphysis and mild cranial sclerosis. It is one of the causes of an Erlenmeyer flask deformity. The flared metaphyses are relatively lucent.
The patients are often asymptomatic, although genu valgus deformity may be a feature.
Where there is cranial involvement, it is termed craniometaphyseal dysplasia.
Differential diagnosis
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1. Beighton P. Pyle Disease (Metaphyseal Dysplasia). J Med Genet. 1987;24(6):321-4. doi:10.1136/jmg.24.6.321 - Pubmed
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2. Heselson N, Raad M, Hamersma H, Cremin B, Beighton P. The Radiological Manifestations of Metaphyseal Dysplasia (Pyle Disease). Br J Radiol. 1979;52(618):431-40. doi:10.1259/0007-1285-52-618-431 - Pubmed
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3. Narayananan V, Ashok L, Mamatha G, Rajeshwari A, Prasad S. Pyle's Disease: An Incidental Finding in a Routine Dental Patient. Dentomaxillofac Radiol. 2006;35(1):50-4. doi:10.1259/dmfr/44987850 - Pubmed
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