Skip to main content
. 2018 Oct 23;107(12):2059–2065. doi: 10.1111/apa.14587

Figure 1.

Figure 1

Characteristic features of MPS I. Facial expressions of a 16‐month‐old MPS I Hurler patient (A,B); gibbus in a 12‐month‐old MPS I Hurler patient (C); hepatosplenomegaly and inguinal hernia in a three‐month‐old patient with MPS I Hurler (D); claw hands in an 18‐month‐old MPS I Hurler patient pre‐HSCT (E); A five‐year‐old patient newly diagnosed with MPS I Hurler–Scheie; note that the facial expressions are not typical (F); umbilical hernia and gibbus in a four‐year‐old MPS I Hurler–Scheie patient on ERT (G); paraparesis in a 40‐year‐old MPS I Scheie patient (H). ERT, enzyme replacement therapy; HSCT, haematopoietic stem cell transplantation; MPS I, mucopolysaccharidosis type I. Informed consent was obtained from all individuals or their guardians.