1997
Preauricular skin defects. A consequence of a persistent ectodermal groove
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Cited by 34 publications
(39 citation statements)
References 12 publications
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“…Our patient’s skin lesions differ to previously described skin lesions of FFDD in both location and the presence of the hair collar. Other authors have noted the same differences in their patients 13,16,17 . We propose these patients may constitute a distinct entity and are best considered as aplasia cutis congenita, not necessarily part of the FFDD.…”
Section: Discussionsupporting
confidence: 53%
“…Our patient’s skin lesions differ to previously described skin lesions of FFDD in both location and the presence of the hair collar. Other authors have noted the same differences in their patients 13,16,17 . We propose these patients may constitute a distinct entity and are best considered as aplasia cutis congenita, not necessarily part of the FFDD.…”
Section: Discussionsupporting
confidence: 53%
“…While one investigator found elastic fibres to be absent in a preauricular lesion with a hair collar 13 our patient showed an increase in elastic tissue. Biopsies of two of 10 patients with preauricular lesions, many with a hair collar, showed flattened atrophic epidermis with replacement of dermis by loose connective tissue and notably absent adnexal structures 16 . Despite some differences in the dermal changes the epidermal and adnexal alterations are very similar.…”
Section: Discussionmentioning
confidence: 91%
“…It is postulated that defects in FFDD arise from incomplete ectoderm closure at facial embryonic fusion lines . Histologic examination of FFDD lesions shows similar features to membranous ACC, supporting the hypothesis that FFDD and ACC share an analogous pathogenesis …”
Section: Discussionmentioning
confidence: 72%
“…In five families, two members were affected, whereas three members belonging to three generations were affected in one family ( Fig. 2) The mode of inheritance is consistent with an autosomal dominant disorder in four families (1,3,4,6). In the other two families (2,5), the mode of inheritance is hard to ascertain.…”
Section: Case Reportsmentioning
confidence: 77%
