Genodermatoses

被引：10

作者：

Babu, N. Aravindha ^{[1
]}

Rajesh, E. ^{[1
]}

Krupaa, Jayasri ^{[1
]}

Gnananandar, G. ^{[1
]}

机构：

[1] Bharath Univ, Sree Balaji Dent Coll & Hosp, Dept Oral pathol & Microbiol, Chennai, Tamil Nadu, India

来源：

JOURNAL OF PHARMACY AND BIOALLIED SCIENCES | 2015年 / 7卷 / 05期

关键词：

Benign; dyskeratosis congenital; ectodermal dysplasia; Ehlers-Danlos syndrome; epidermolysis bullosa; hereditary; hidrotic ectodermal dysplasia; hypohidrotic ectodermal dysplasia; incontinentia pigmenti; intraepithelial-dyskeratosis; keratosis follicularis; multiple hamartoma syndrome; pachyonychia congenital; Peutz-Jeghers syndrome; tuberous sclerosis; Warty dyskeratoma; white sponge nevus; xeroderma pigmentosum;

D O I：

10.4103/0975-7406.155903

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

Genodermatoses are an inherited disorder, present with multisystem involvement. Help us to identify regular mutations and appalling skin diseases with recessive inheritance. Genetic heterogeneity is very common, and molecular diagnosis requires a broad effort. Recurrent mutations in unrelated families were seen in families with xeroderma, Griscelli. It seems likely that eventually oligonucleotide arrays will replace most other methods for routine mutation scanning of the more common diseases and planned sequencing will be increasingly used for rarer diseases.

引用

页码：S203 / S206

页数：4

共 20 条

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