Downloads: 0
Case Studies | Pediatrics | India | Volume 11 Issue 6, June 2022
Rare Case Report on Incontinentia Pigmenti
Dr. Tinkal Patel | Dr. Devavrat Bhide | Dr. Panna Patel | Dr. Apoorva Shah
Abstract: Incognentiapigmenti is a neurocutaneous syndrome. It is a x - linked dominant disorder. It is a rare, inheritable, multisystem ectodermal disorder. Pathogenic IKBKG gene or 47, XXY karyotyping seen in female X - inactivation (45, X) seen. Most commonly involved organ is skin. Other systems involved are CNS, ocular, dental and hair.
Keywords: Incontinentia Pigmenti, neurocutaneous syndrome
Edition: Volume 11 Issue 6, June 2022,
Pages: 1559 - 1560
How to Cite this Article?
Dr. Tinkal Patel, Dr. Devavrat Bhide, Dr. Panna Patel, Dr. Apoorva Shah, "Rare Case Report on Incontinentia Pigmenti", International Journal of Science and Research (IJSR), Volume 11 Issue 6, June 2022, pp. 1559-1560, https://www.ijsr.net/get_abstract.php?paper_id=MR22623230731
How to Share this Article?
Similar Articles with Keyword 'syndrome'
Downloads: 0
Case Studies, Pediatrics, India, Volume 11 Issue 6, June 2022
Pages: 847 - 850A Case Report on Systemic Lupus Erythematosis, Lupus Nephritis, Acute Pancreatitis, Posterior Reversible Encephalopathy Syndrome (PRES), Macrophage Activating Syndrome (MAS)
S. Mohamed Ashik Ali | P. Muhammed Nishad | A. Priya [3] | K. Arun Chander
Downloads: 2 | Weekly Hits: ⮙1 | Monthly Hits: ⮙1
Student Project, Pediatrics, India, Volume 11 Issue 4, April 2022
Pages: 618 - 620Incidence and Risk Factors of Respiratory Distress Syndrome in Special Neonatal Care Unit
U Sai Anirudh Goud | G Rushmitha Krishna | L Rajesh [3] | V Gowtham Krishna