Protein-losing enteropathy and multiple vasculature dysplasia in LZTR1-related Noonan syndrome: A case report and review of literature

Figure 1 Pedigree and characteristic appearance of the patient. A: In the pedigree of the patient’s family, patients are represented in black, the arrow represents the proband, which is the patient discussed in this case; B: Characteristic craniofacial appearance of widely spaced eyes in adolescence and infant. In addition, the distal phalanx of the left little finger was absent since birth. The patient was informed and agreed to publish the photos (Supplementary material).