Explanipedia

Restless Jaw Syndrome: A Novel Possible Regional Anatomic Variant of Restless Leg Syndrome Open

Sasankoti Mohan Ravi Prakash, I. Gupta · 2025

Idiopathic Fibrillary Glomerulonephritis: A Case Report Highlighting Diagnostic and Management Challenges Open

Emin Gayibov, I. Gupta · 2025

Fibrillary glomerulonephritis (FGN) is a rare glomerular disease characterized by non-branching fibrils within the glomerular basement membrane, often leading to progressive renal dysfunction. Despite advances in diagnostic methods, includ…

Mesenchymal Wnts are required for morphogenetic movements of calvarial osteoblasts during apical expansion Open

Nikaya Polsani, Theodora Yung, Evan Thomas, Melissa Phung-Rojas, I. Gupta , et al. · 2024

Apical expansion of calvarial osteoblast progenitors from the cranial mesenchyme (CM) above the eye is integral to calvarial growth and enclosure of the brain. The cellular behaviors and signals underlying the morphogenetic process of calv…

Apical expansion of calvarial osteoblasts and suture patency is dependent on fibronectin cues Open

Xiaotian Feng, Helen Molteni, Megan Gregory, Jennifer Lanza, Nikaya Polsani , et al. · 2024

The skull roof, or calvaria, is comprised of interlocking plates of bones that encase the brain. Separating these bones are fibrous sutures that permit growth. Currently, we do not understand the instructions for directional growth of the …

Mesenchymal Wnts are required for morphogenetic movements of calvarial osteoblasts during apical expansion Open

Nikaya Polsani, Theodora Yung, Evan Thomas, Melissa Phung-Rojas, I. Gupta , et al. · 2023

Apical expansion of calvarial osteoblast progenitors from the cranial mesenchyme (CM) above the eye is integral for calvarial growth and enclosure of the brain. The cellular behaviors and signals underlying the morphogenetic process of cal…

Angioma Serpiginosum with Soft Tissue Hypertrophy and Palmar Involvement: A Rare Presentation Open

I. Gupta, Surabhi Dayal, Priyadarshini Sahu, Rajeev Sen · 2023

Focal Dermal Hypoplasia (Goltz Syndrome) Open

I. Gupta, Neha Dhankar, Surabhi Dayal, Meha Tyagi · 2022

Sir, Goltz syndrome, described first by Liebermann in 1935 as “atrophoderma linearis maculosa et papillomatosis congenitalis”, is a rare mesoectodermal dysplasia with X-linked dominant inheritance mainly affecting females and lethal in mal…

Griscelli Syndrome Type 3 in Siblings Open

I. Gupta, Neha Dhankar, Surabhi Dayal, Sonia Chhabra · 2022

Risk and safe practice pattern for ophthalmologists in seropositives Open

Brij K. Gupta, Kanav Gupta, I. Gupta · 2020

Objective: To analyze the risk involved in eye surgery and follow safe practice pattern in Seropositive [Hepatitis B (HBV), Hepatitis C(HCV) and Human Immuno-deficiency Virus (HIV)] cases.Materials and Methods: This retrospective analysis …

Bilateral systematized porokeratotic eccrine ostial and dermal duct nevus Open

I. Gupta, Surabhi Dayal, Sanjay Kumar · 2020

Guttate leukoderma in darier disease: A rare presentation Open

I. Gupta, Surabhi Dayal, Sanjay Kumar · 2019

Sir, A 50-year-old female presented with chief complaints of asymptomatic multiple red-brown raised keratotic lesions along with hypopigmented lesions all over body since 20 years. Keratotic lesions started from face and gradually involved…

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Monika Fleckenstein, Paul Mitchell, K. Bailey Freund, Srinivas R. Sadda, Frank Holz , et al. · 2018

Keratosis pilaris spinulosa decalvans in Siblings: A Rare Cause of Scarring Alopecia Open

Pallavi Goya, I. Gupta · 2016

Keratosis follicularis spinulosa decalvans (KFSD) i s a hereditary disorder of the hair follicle which presents with scarring alopecia and follicular papu les affecting the scalp and other areas of the body . Being X-linked it is more comm…

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