Familial progressive hypermelanosis in Indian monozygotic twins.

Abstract:

:Familial hyperpigmentation, or melanosis universalis hereditaria, is a rare hyperpigmentary disorder with onset in infancy. Here, we describe monozygotic twins with similar pattern of progressive hyperpigmentation with onset in early neonatal period without any family history. Histopathological examination showed increased melanin throughout the epidermis. Although hereditary defects may influence melanogenesis resulting in a pigmentary anomaly, the pathogenesis of hyperpigmentation in this case remains unclear.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Gupta N,Sharma MC,Ramam M,Kabra M

doi

10.1111/j.1525-1470.2010.01361.x

subject

Has Abstract

pub_date

2011-01-01 00:00:00

pages

62-5

issue

1

eissn

0736-8046

issn

1525-1470

journal_volume

28

pub_type

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