Skip to main content
Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: LipoDDx: a mobile application for identification of rare lipodystrophy syndromes

Fig. 2

Different screens of LipoDDx®. a First screen. b Screen with dichotomous question. c Screen with a picture of a characteristic sign of some lipodystrophies. d Screen with a drop-down menu for choosing different signs. e Screen of a final results indicating the possible lipodystrophy subtype. In this case, information is given about the genes that should be sequenced and also links to OMIM, and bibliographic references

Back to article page