TWO CASES OF PESUTZ- JEGHERS SYNDROME IN ONE FAMILY

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LAHSAEE S.; POURLASHKARI M.

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Journal: Journal of Shahid Sadoughi University of Medical Sciences Year:2000 | Volume:8 | Issue:4 Page(s): 79-81

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Information Journal Paper

Title

TWO CASES OF PESUTZ- JEGHERS SYNDROME IN ONE FAMILY

Author(s)

LAHSAEE S. | | POURLASHKARI M. | Issue Writer Certificate

Keywords

PESUTZ - JEGHERS SYNDROMEQ4

CUTANEOUS PIGMENTATIONQ4

POLYPOSISQ4

GASTROINTESTINAL MALIGNANCIESQ4

AUTOSOMAL DOMINANTQ3

Abstract

The Pesutz- Jeghers Syndrome, Phenotypically is characterized by mucocutaneous pigmentation and Hamartomatous POLYPOSIS. The disease is an AUTOSOMAL DOMINANT disease with variable expression and incomplete penetrance. Moreover, affected patients are at increased risk of gastrointestinal and other malignancies. This is a report of two cases of Pesutz- Jeghers Syndrome in father and his son. The father died from gastrointestinal malignancy at the age of 42. The second case is suffering from gastric pain now. Periodical observations and recurrent examinations are helpful in diagnosis of malignant degenerations in this syndrome. Malignant precocious transformation is a rare finding in his father and lower lid pigmentation is a new finding in this case.

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APA: Copy

LAHSAEE, S., POURLASHKARI, M.. (2000). TWO CASES OF PESUTZ- JEGHERS SYNDROME IN ONE FAMILY. JOURNAL OF SHAHID SADOUGHI UNIVERSITY OF MEDICAL SCIENCES, 8(4), 79-81. SID. https://sid.ir/paper/36111/en

Vancouver: Copy

LAHSAEE S., POURLASHKARI M.. TWO CASES OF PESUTZ- JEGHERS SYNDROME IN ONE FAMILY. JOURNAL OF SHAHID SADOUGHI UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2000;8(4):79-81. Available from: https://sid.ir/paper/36111/en

IEEE: Copy

S. LAHSAEE, M. POURLASHKARI, “TWO CASES OF PESUTZ- JEGHERS SYNDROME IN ONE FAMILY,” JOURNAL OF SHAHID SADOUGHI UNIVERSITY OF MEDICAL SCIENCES, vol. 8, no. 4, pp. 79–81, 2000, [Online]. Available: https://sid.ir/paper/36111/en

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