Case report highlights a rare combination of Dyggve Melchior Clausen disease and Smith Mccort dysplasia in an individual, suggesting unique clinical significance.
Dyggve Melchior Clausen (DMC) syndrome is an unusual form of uncommon autosomal recessive skeletal dysplasia.After its first occurrence in 1962, there has only been a hundred case reports to date with a mean incidence rate of0.1 per million.1 This article presents an account on a rare case report of Dyggve-MelchiorClausen disease combined with Smith Mccort Dysplasia.
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Krishnan et al. (2025) studied this question.
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