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. 2020 Aug 12;10(8):582. doi: 10.3390/diagnostics10080582

Figure 1.

Figure 1

(A) Patient (right) at age 13 years and her mother (left) show typical features of NS, note the short stature and common facial features (ptosis, hypertelorism, downslanting palpebral fissures and low-set ears) and a short webbed neck; (B) pedigree of the family in which NS cosegregated with the recurrent PTPN11 mutation.