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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