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. 2002 Nov;87(5):444–445. doi: 10.1136/adc.87.5.444

Familial neurofibromatosis microdeletion syndrome complicated by rhabdomyosarcoma

A Lampe 1, G Seymour 1, P Thompson 1, A Toutain 1, S Lynch 1
PMCID: PMC1763076  PMID: 12390929

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Figure 1 .

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.


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