We describe four patients with focal dermal hypoplasia (FDH): a girl with classic FDH, a boy with cutaneous findings, an infant with severe multisystem disease, and the infant's mother, who had previously undiagnosed FDH. These patients illustrate the classic cutaneous manifestations of FDH and the variations that can exist within a family.
|Original language||English (US)|
|Number of pages||5|
|Journal||Journal of the American Academy of Dermatology|
|Issue number||5 II|
|State||Published - 1993|
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