Orthodontic Perspective on Marfan Syndrome: A Unique Case Report
Marfan syndrome is considered a relatively rare genetic disorder that affects the connective tissues in the body. It is caused by a specific mutation in the Fibrillin 1 (FBN1) gene, which is a critical component of microfibrils. The elastic fibres in various connective tissues, composed of microfi...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
JCDR Research and Publications Private Limited
2023-11-01
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Series: | Journal of Clinical and Diagnostic Research |
Subjects: | |
Online Access: | https://www.jcdr.net/articles/PDF/18668/65591_CE[Ra1]_F(SS)_QC(SD_RDW_IS)_PF1(HB_SS_OM)_PFA_NC(HB_KM)_PN(KM).pdf |