A CASE SERIES OF PHYLLOID HYPOMELANOSIS-Reference-Cited by-同舟云学术

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A CASE SERIES OF PHYLLOID HYPOMELANOSIS

Published:2021-07-15 Issue: Volume: Page:8-9
ISSN:
Container-title:PARIPEX INDIAN JOURNAL OF RESEARCH
language:en
Short-container-title:PIJR

Author:

Agrawal S.N.¹,M Varma Nisha²,Patil Manali,Bhagwat Mohini³

Affiliation:

1. PROF AND HOD Dermatology Department Dr PDMC Hospital Amravati.

2. Jr2 DERMATOLOGY Department, Dr PDMC Hospital Amravati.

3. (JR 3 ) Dermatology department , Dr PDMC hospital, Amravati.

Abstract

THE PHYLLOID HYPOMELANOSIS is a defined as a distinct syndrome consisting of achromic phylloid skin lesions in combination with extracutaneous anomalies such as mental retardation , agenesis of corpus callosum , conductive hearing loss ,coloboma and various skeletal defects[1].

Publisher

World Wide Journals

Reference12 articles.

1. Happle R. Phylloid hypomelanosis is closely related to mosaic trisomy 13. Eur J Dermatol. 2000;10(7):511-512.

2. Happle R. Mosaicism in human skin. Understanding the patterns and mechanisms. Arch Dermatol 1993; 129: 1460-1470.

3. Happle R. Pigmentary patterns associated with human mosaicism: a proposed classification. Eur J Dermatol 1993; 3: 170-174.

4. Happle R. Phylloid hypomelanosis is closely related to mosaic trisomy 13. EurJ Dermatol 2000; 10: 511-512.

5. Happle R. Phylloid hypomelanosis and mosaic trisomy 13: a new etiologically defined neurocut£meous syndrome. Hautarzt 2001; 52: 3-5.

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