Puetz-Jeghers Syndrome Involving Appedix

Authors

  • Raysan F. Al-Fayadh 00000
  • Ali Jaliel Awad, 00000

Keywords:

0000

Abstract

This is an autosomal dominant disease. The gene STK11 on chromosome 19 has been found in proportions of patients with this condition, this consists of: A-Intestinal hamartomatosis. B-Melanosis of the oral mucous membrane and the lips.

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Published

2010-06-30

Issue

Vol. 6 No. 1 (2010): Vol 6 No 1 (2010): Vol 6 No 1 (2010): AL-Kindy College Medical Journal

Section

Research Articles

License

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

How to Cite

1.
Al-Fayadh RF, Awad, AJ. Puetz-Jeghers Syndrome Involving Appedix. Al-Kindy Col. Med. J [Internet]. 2010 Jun. 30 [cited 2024 Nov. 19];6(1):138-9. Available from: https://jkmc.uobaghdad.edu.iq/index.php/MEDICAL/article/view/712

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