Association of Abo Blood Groups and Rh Factor with Sagittal and Vertical Skeletal Malocclusion- An Observational Study

Autor: Sampath Aravind, Duraisamy Sangeetha, Rajaram Krishnaraj, K Ravi, S Srinivas, K Ashok Priya

Publikováno v: Journal of Clinical and Diagnostic Research, Vol 16, Iss 7, Pp ZC01-ZC05 (2022)

Introduction: Various studies have proved the association between several disease including dental crowding, malocclusion and craniofacial deformities with blood group. Certain skeletal problems in sagittal plane are heritable and the skeletal muscle

Externí odkaz: https://doaj.org/article/92165792e76c4572a8318848d52a686f

A novel homozygous missense mutation in exon 3 at codon 42 c.125G>A (p.Arg42His) in the PROC gene causing protein C deficiency and presenting as neonatal purpura fulminans.

Autor: Francis A; Department of Dermatology & Venereology, Government Medical College, Trivandrum, India., George AE; Department of Dermatology & Venereology, Government Medical College, Trivandrum, India., Ashok P; Department of Dermatology & Venereology, Government Medical College, Trivandrum, India., Chandran R; Department of Dermatology & Venereology, Government Medical College, Trivandrum, India.

Publikováno v: Indian journal of dermatology, venereology and leprology [Indian J Dermatol Venereol Leprol] 2024 Apr 23, pp. 1-3. Date of Electronic Publication: 2024 Apr 23.