Significance of Multimodal Imaging in Diagnosis of HJMD
Agrima Bhatt, Rajasthan University What is HJMD? HJMD or Hypotrichosis with macular dystrophy is an autosomal syndrome commonly found in young children. It is caused by a mutation in a gene CDH3, responsible for encoding a protein in hair follicles, and the retinal pigment epithelium (RPE). CDH3 encodes a glycoprotein known as P-cadherin, found at […]
