1992
DOI: 10.1016/s0190-9622(08)80224-1
|View full text |Cite
|
Sign up to set email alerts
|

Unilateral dermatomal pigmentary dermatosis: A variant dyschromatosis?

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

3
8
0

Year Published

1995
1995
2014
2014

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 10 publications
(11 citation statements)
references
References 9 publications
3
8
0
Order By: Relevance
“…In the present case, the skin lesions of this patient were segmental, and multiple blue naevi and cherry angiomas were seen in and around the skin lesions. The cases reported by Hara et al . exhibited segmentally distributed skin lesions, similar to the present case.…”
Section: Reportsupporting
confidence: 90%
See 2 more Smart Citations
“…In the present case, the skin lesions of this patient were segmental, and multiple blue naevi and cherry angiomas were seen in and around the skin lesions. The cases reported by Hara et al . exhibited segmentally distributed skin lesions, similar to the present case.…”
Section: Reportsupporting
confidence: 90%
“…is a rare disorder, characterized by the presence of hyperpigmented and hypopigmented macules in a localized area. Only a few cases have been reported . We report a case of localized dyschromatosis associated with multiple blue naevi and cherry angiomas, which we believe to be the first such case reported.…”
mentioning
confidence: 76%
See 1 more Smart Citation
“…It is differentiated from segmental neurofibromatosis and partial unilateral lentiginosis by the mottled hyperpigmentation and hypopigmentation. [27] Indian Journal of Dermatology, Venereology, and Leprology | January-February 2013 | Vol 79 | Issue 1 …”
Section: Unilateral Dermatomal Pigmentary Dermatosis (Udpd)mentioning
confidence: 99%
“…414 Onset is in early childhood, usually the first few months of life, with involvement being most prominent on the trunk and extremities. [456][457][458][459][460] The gene responsible maps to chromosome 6q24.2-q25.2. Clinical variants have been described.…”
Section: Dyschromatosis Universalis Hereditariamentioning
confidence: 99%