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Figure 1 | Orphanet Journal of Rare Diseases

Figure 1

From: TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families

Figure 1

X-rays of some of the cases described. A, B, C, pelvis, legs and lateral spine of case 5 (MD-SMDK bridging phenotype); D, case 8 (MD); E, F, AP spine and pelvis of case 16 (SMDK); G, H, lateral spine and pelvis of patient 18 (SMDK); I, AP spine and pelvis of case 19 (SMDK); J, AP spine and pelvis of case 20 (SMDK); K, AP spine and pelvis of case 21 (SMDK); L, lateral spine and pelvis of case 26, who had some minor spinal changes and no metaphyseal involvement.

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