1982
DOI: 10.1001/archderm.1982.01650190044017
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Reticulate Pigmented Anomaly of the Flexures

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Cited by 17 publications
(4 citation statements)
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“…Without examining our patient's father and brother, we cannot be completely certain that they had Dowling Degos Disease but it would appear from the history that they probably did. This would represent four generations of Dowling Degos Disease and corroborate the evidence of Brown (1982) that this genodermatosis is inherited in an autosomal dominant manner.…”
Section: Discussionsupporting
confidence: 78%
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“…Without examining our patient's father and brother, we cannot be completely certain that they had Dowling Degos Disease but it would appear from the history that they probably did. This would represent four generations of Dowling Degos Disease and corroborate the evidence of Brown (1982) that this genodermatosis is inherited in an autosomal dominant manner.…”
Section: Discussionsupporting
confidence: 78%
“…We feel that this may represent an association of seborrhoeic warts and Dowling Degos Disease. The presence of this condition in four generations confirms the autosomal dominant inheritance reported by Brown (1982).…”
supporting
confidence: 81%
“…Genetics DDD, HS, and KAR have all been shown to be autosomal dominant conditions (Brown, 1982;Kikuchi, 1982;Griffiths, 1976), beginning in childhood.…”
Section: Karmentioning
confidence: 99%
“…Dowling-Degos disease (Reticulate pigmented anomaly of the flexures) is an autosomal dominant condition characterized by reticulate brownish pigmentation of the flexures (5)(6)(7). The disorder has a late onset and is frequently accompanied with pigmented comedones and acneform scars.…”
Section: Discussionmentioning
confidence: 99%