合計: 2 |
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PMID (PMCID) | ||
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12220269 |
MIXED_SAMPLE | Infant, Newborn |
Erythrokeratodermia variabilis with erythema gyratum repens-like lesions. | ||
Landau M, Cohen-Bar-Dayan M, Hohl D, Ophir J, Wolf CR, Gat A, Mevorah B. Pediatr Dermatol. 2002;19(4):285-92. |
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The differential diagnoses of the following dermatoses with an erythematous and a hyperkeratotic component are discussed: erythrokeratodermia variabilis (Mendes da Costa), progressive symmetric erythrokeratoderma (Gottron), loricrin keratoderma, erythrokeratoderma en cocardes (Degos), Netherton syndrome, keratitis-ichthyosis-deafness (KID) syndrome, erythrokeratolysis hiemalis (Oudtshoorn disease), and nonbullous congenital ichthyosiform erythroderma. | ||
11703298 |
MIXED_SAMPLE | Child |
Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby. | ||
Matsumoto K, Muto M, Seki S, Saida T, Horiuchi N, Takahashi H, Ishida-Yamamoto A, Iizuka H. Br J Dermatol. 2001;145(4):657-60. |
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Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby. |