Familial neurofibromatosis microdeletion syndrome complicated by rhabdomyosarcoma

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Figure 1 .

(A) Case 1, aged 12 months: broad and coarse face with full cheeks and possible hypertelorism. (B) Case 2, age 4½12: round and broad face with full cheeks, depressed nasal bridge, anteverted nares and micrognathia; note hypertelorism with left divergent squint. (C) Case 3, aged 15 months: full cheeks, depressed nasal bridge, anteverted nares, micrognathia and epicanthic folds.