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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Untangling neurodevelopmental disorders in the adulthood: a movement disorder is the clue

Fig. 1

Detected mutations in SON, ZMYND11, DNMT1 and YY1 and related brain imaging features. a Protein changes related to the described mutation in SON, ZMYND11, DNMT1 and YY1. b, c 1,5 Tesla brain MRI-Imaging from patient 2 (ZMYND11-related disease) showing global atrophy as well as turricephaly; b T1-axial sequence, c T2 dark-fluid coronal sequence. d, e 1,5 Tesla brain MRI-Imaging from patient 3 (YY1-related disease) showing a normal appearance of basal ganglia and multiple unspecific white matter lesions; T2 dark-fluid axial sequences

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