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Phylloid hypermelanosis is a rare form of pigmentary mosaicism that has been reported only a few times in the literature (1–6). While phylloid hypomelanosis is linked to trisomy 13, the cause of phylloid hypermelanosis is more obscure (5, 7–13). We describe here a case of phyl-loid hypermelanosis associated with mild developmental delay, cicatricial alopecia, hearing loss and polythelia. CASE REPORT

Phylloid Hypermelanosis in a Child with Psychomotor Delay, Cicatricial Alopecia, Hearing Loss and Polythelia