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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: The phenotypic spectrum of terminal 6q deletions based on a large cohort derived from social media and literature: a prominent role for DLL1

Fig. 2

Clinical photographs of individuals with a terminal 6q deletion of at least 7.9 Mb (including the HI-gene PRKN) at the age of 8 years (Id012), 2 years (Id111), 10 years (Id222), 6 years (Id038), 1 year (Id108) and 8 years (Id224). Note the hypertelorism and dysplastic outer ears in most individuals. Written consent was given to the authors to publish patients’ photographs

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172