Results 81 to 90 of about 5,283 (174)

[Peutz-Jeghers syndrome].

open access: yesRevista de gastroenterologia de Mexico, 2004
Peutz-Jeghers syndrome is an autonomic dominant disease characterized by hamartomatous polyps and mucocutaneous hyperpigmentation. We present 16 cases; females were more affected. The most common presenting complaints were of gastrointestinal tract. All polyps found were hamartomatous with general distribution through gastrointestinal tract. Endoscopic
Roberto, Cervantes Bustamante   +6 more
openaire   +1 more source

Severe Iron Deficiency Anemia in a Jehovah's Witness diagnosed with Peutz-Jeghers Syndrome. [PDF]

open access: yesJ Brown Hosp Med
Gulla V   +5 more
europepmc   +1 more source

Adrenocortical Carcinoma in Peutz-Jeghers Syndrome With a Rare STK11 Pathogenic Germline Variant: A Case Report. [PDF]

open access: yesCancer Rep (Hoboken)
Ishida T   +14 more
europepmc   +1 more source

Peutz -Jeghers syndrome (PJS) [PDF]

open access: yesInternational Journal of Clinical Practice, 2017
openaire   +2 more sources

Familial pediatric Peutz-Jeghers syndrome with recurrent intussusception: case report and literature review. [PDF]

open access: yesFront Pediatr
Sahli S   +7 more
europepmc   +1 more source

Acute intestinal intussusception revealing Peutz-Jeghers Syndrome in a 16-year-old male: a case report. [PDF]

open access: yesInt J Surg Case Rep
Atri S   +5 more
europepmc   +1 more source

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