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. 2020 Apr 20;97(6):890–901. doi: 10.1111/cge.13749

FIGURE 1.

FIGURE 1

Features from selected individuals with Primrose syndrome. (A) Faces from youngest to oldest at age 1.5 years (A), 2.5 years (B), 3 years (C), 4 years (D), 4 years (E), 5 years (F), 6 years (G), 8 years (H), 9 years (I), 11 years (J), 12 years (K), 13 years (L), 18 years (M), 31 years (N), 33 years (O), and 53 years (P). The patient identification number is indicated underneath the panels. (B) Other clinical features include alobar calcified ear (1), calcified ear on X‐ray (2), incomplete extension of fingers and small nails (3), joint hypermobility (4), distal muscle wasting in an adult (5), markedly small and thin nails (6), and malformed callosal body (7) [Colour figure can be viewed at wileyonlinelibrary.com]