Hypomelanosis of Ito: A Genetic Mosaicism
Evidence purporting that the so-called hypomelanosis of Ito (HI) syndrome does not exist as a distinct multisystem birth defect is presented by geneticists and dermatologists at Bad Salzschlirf, and Philipp University of Marburg, Germany.
Main Author: | J Gordon Millichap |
---|---|
Format: | Article |
Language: | English |
Published: |
Pediatric Neurology Briefs Publishers
1999-09-01
|
Series: | Pediatric Neurology Briefs |
Subjects: | |
Online Access: | https://www.pediatricneurologybriefs.com/articles/1990 |
Similar Items
-
Hypomelanosis of Ito: report of two cases
by: Mohammad Abid Keen
Published: (2015-10-01) -
A Female Child with Skin Lesions and Seizures Case report of Incontinentia Pigmenti
by: Sana Al-Zuhaibi, et al.
Published: (2009-08-01) -
An interesting coexistence of multifocal hypertrichosis and hirsutism in hypomelanosis of ito
by: Vibhu Mendiratta, et al.
Published: (2019-01-01) -
HYPOMELANOSIS OF ITO WITH EPILEPSY: TWO CASES IN CLINICAL PRACTICE
by: M. B. Mironov, et al.
Published: (2016-08-01) -
Hypomelanosis of Ito with an unusual pulmonary abnormality in an infant
by: Ramesh Y Bhat, et al.
Published: (2014-01-01)