International Journal of Science and Research (IJSR)

International Journal of Science and Research (IJSR)
Since Year 2012 | Open Access | Fully Refereed | Peer Reviewed

ISSN: 2319-7064




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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

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