Autor: |
Vaishali Wankhade, Vrutika Hasmukh Shah, Rajesh P Singh, Jayesh Mukhi |
Jazyk: |
angličtina |
Rok vydání: |
2019 |
Předmět: |
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Zdroj: |
Indian Journal of Paediatric Dermatology, Vol 20, Iss 3, Pp 267-270 (2019) |
Druh dokumentu: |
article |
ISSN: |
2319-7250 |
DOI: |
10.4103/ijpd.IJPD_98_18 |
Popis: |
Phacomatosis pigmentokeratotica is a rare form of cutaneous mosaicism characterized by epidermal nevus usually nevus sebaceous, papular speckled lentiginous nevus, and extracutaneous anomalies. This type of twin-spot phenomenon (didymosis) is due to postzygotic crossing-over resulting in two homozygous daughter cells, representing the stem cells of the two distinct types of nevi and leading to additional extracutaneous defects. We report a case of this rare syndrome in a 4-year-old male child associated with skeletal anomalies. |
Databáze: |
Directory of Open Access Journals |
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