Open AccessGREENBERG'S DYSPLASIA- A RARE GENETIC CONDITION
Author(s) -
S Sundari,
J Harish
Publication year - 2020
Publication title -
international journal of scientific research
Language(s) - English
Resource type - Journals
ISSN - 3046-5206
DOI - 10.36106/ijsr/5729297
Subject(s) - genetics , dermatology , medicine , biology
Greenberg’s Dysplasia, also known as Hydrops-Ectopic calcification-Moth-Eaten (HEM) Skeletal Dysplasia, is a rare autosomal recessive osteochondrodysplasia, caused by mutation in the Lamin B Receptor (LBR) Gene, on chromosome 1q42.
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