A rare association of incontinentia pigmenti with congenital heart disease in a newborn
Introduction: Incontinentia pigmenti (IP) is a rare genodermatosis. It classically has manifestations of linear vesicular lesions, evolving into verrucous lesions within few weeks, followed by a peculiar swirled pigmentation lasting for many years. In addition, IP can affect other ectodermal tissues...
Saved in:
Main Authors: | Asha Gowrappala Shanmukhappa (Author), Mounica Chimbili (Author), Leelavathy Budamakuntla (Author), Shilpa Kanathur (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2021-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A rare case of neurocutaneous disorders of the newborn: Incontinentia pigmenti
by: Melek Aslan Kayiran, et al.
Published: (2018) -
Incontinentia pigmenti
by: Hegde Sundeep, et al.
Published: (2006) -
Incontinentia pigmenti
by: Claudia Schermann Poziomczyk, et al.
Published: (2014) -
Incontinentia pigmenti
by: Motamedi Mohammad Hosein, et al.
Published: (2010) -
Incontinentia Pigmenti in a Newborn. A Case Report
by: Yahiris García Rodríguez, et al.
Published: (2015)