Results 71 to 80 of about 2,571 (160)

Peutz–Jeghers syndrome – Be in need of vigilance: A case report

open access: yesJournal of Family Medicine and Primary Care
Peutz–Jeghar syndrome (PJS) is an inherited condition that puts people at an increased risk for developing hamarotmatous polyps in the digestive tract as well as cancers of the breast, colon, rectum, pancreas, stomach, testicles, ovaries, lung and cervix.
Vandana S. Tomey   +3 more
doaj   +1 more source

Você conhece esta Síndrome? Do you know this syndrome?

open access: yesAnais Brasileiros de Dermatologia, 2010
Síndrome de Laugier-Hunziker é caracterizada por hiperpigmentação macular adquirida, idiopática das mucosas oral e genital, que pode estar associada à melanoníquia longitudinal.
Priscilla Maria Rodrigues Pereira   +4 more
doaj   +1 more source

Laugier-Hunziker syndrome – a rare cause of acquired hyperpigmentation

open access: yesPrzegląd Dermatologiczny, 2022
Mariana Karwan, Piotr Brzeziński
doaj   +1 more source

Poster Sessions

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Publication Only

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: clinical and molecular characterization of a new contiguous gene syndrome

open access: yesGenetics and Molecular Biology, 2011
The Peutz-Jeghers syndrome (PJS) is an autosomal-dominant hamartomatous polyposis syndrome characterized by mucocutaneous pigmentation, gastrointestinal polyps and the increased risk of multiple cancers.
Josiane Souza   +5 more
doaj  

Mucocutaneous pigmentation due to zinc deposition

open access: yesThe Lancet, 2000
JE Greenberg   +3 more
openaire   +1 more source

Home - About - Disclaimer - Privacy