Metabolic syndrome coexists with adult Léri–Weill dyschondrosteosis: A case report
Abstract Léri–Weill dyschondrosteosis (LWD) is usually caused by haploinsufficiency of the short stature homeobox‐containing gene (SHOX). The clinical manifestation of this disease is a classic triad, which are short stature, mesomelia and Madelung deformity. LWD also includes other features, such a...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley
2021-03-01
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| Series: | Journal of Diabetes Investigation |
| Subjects: | |
| Online Access: | https://doi.org/10.1111/jdi.13350 |