Ipsita Mohapatra

Beyond the Extra Digit: A Rare Case of Bardet-biedl Syndrome in a 12-Year-Old with Polydactyly, Obesity and Vision Loss

Asha Prakash Mohapatra, Pratyus Patra & Ipsita Mohapatra · Asian Journal of Pediatric Research · 2025

Bardet-Biedl Syndrome (BBS) is a rare multisystem ciliopathy with autosomal recessive inheritance and genetic heterogeneity, characterised by retinal degeneration, post axial polydactyly, renal disease, hypogonadism, central obesity, several dysmorphic features and variable degre...

Open access Research Article 10.9734/ajpr/2025/v15i5444

Nager Syndrome Co-Harboring Mutation Consistent with Stickler Syndrome: A Rare Case Report

Asha Prakash Mohapatra, Ankita Satpathy, Athulya P. U., Leena Das & Ipsita Mohapatra · Asian Journal of Pediatric Research · 2023

Nager syndrome, or preaxial acrofacial dysostosis, is a rare malformation characterized by abnormalities of the craniofacial skeleton and limbs. Although most cases are sporadic and some cases have been demonstrated to have an autosomal dominant or recessive mode of inheritance,...

Open access Research Article 10.9734/ajpr/2023/v13i4293