1966
DOI: 10.1007/bf00502854
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Zur Ultrastruktur und Histochemie der granulösen Degeneration bei bullöser Erythrodermie congénitale ichthyosiforme

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Cited by 14 publications
(3 citation statements)
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“…Therefore, some authors [7][8][9] believe that IH is a clinical variant of BCIE and probably represents a different expression of a pleiotropic domi nant gene [10,11]. This hypothesis is strengthened by the occurrence of both dis eases in the same family [12].…”
Section: Discussionmentioning
confidence: 70%
“…Therefore, some authors [7][8][9] believe that IH is a clinical variant of BCIE and probably represents a different expression of a pleiotropic domi nant gene [10,11]. This hypothesis is strengthened by the occurrence of both dis eases in the same family [12].…”
Section: Discussionmentioning
confidence: 70%
“…Electron microscopy has revealed that the ultra structural features in DEA are similar to those in systematized nevus verrucosus (1,3,10) as well as to those in bullous congenital ichthyosiform erythroderma (4, 5,6,7,8,15,16). It has also revealed the nature of the changes in DEA.…”
Section: Discussionmentioning
confidence: 76%
“…However, distinct keratinosomes are not seen in this disease. Congenital ichthyosiform erythroderma shows clumps of tonofilaments around the nucleus (11). In hyperkeratotic skin.…”
Section: Discussjonmentioning
confidence: 99%