PARC Syndrome
摘要
In their 1990 report, Verloes et al. detail a case where a father and son exhibited generalized alopecia and congenital poikiloderma, resembling Rothmund-Thomson syndrome but with distinct features; the son also presented with cleft palate and Pierre Robin sequence, while the father showed retrognathism with overbite but no palatal defect (Verloes et al. 1990).