Zobrazeno 1 - 10
of 26
pro vyhledávání: '"mucocutaneous hyperpigmentation"'
Publikováno v:
Pigment International, Vol 6, Iss 1, Pp 37-42 (2019)
Vitamin B12 deficiency presents usually with hematologic, gastrointestinal, neurologic, and less commonly, psychiatric, cardiovascular, and dermatological manifestations. A 20-year-old female presented with palmoplantar hyperpigmentation, accentuated
Externí odkaz:
https://doaj.org/article/4f1321c3e8524238a7cc0565718cc09c
Publikováno v:
Indian Journal of Dermatology, Vol 62, Iss 2, Pp 191-194 (2017)
Introduction: Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive potentially life-threatening condition, characterized by glucocorticoid deficiency, preserved aldosterone/renin secretion, and secondary rise in plasma adrenocortico
Externí odkaz:
https://doaj.org/article/44df9752b83943d2a32e9d400d5bb20f
Publikováno v:
Dermatology Practical & Conceptual, Vol 7, Iss 2 (2017)
Laugier-Hunziker syndrome (LHS) is a rare condition characterized by acquired hyperpigmentation involving the lips, oral mucosa, acral surfaces, nails and perineum. While patients with LHS may manifest pigmentation in all of the aforementioned areas,
Externí odkaz:
https://doaj.org/article/a3f3b3e549884c1cac641c6952ab28af
Autor:
Hande Ermiş
Publikováno v:
Volume: 4, Issue: 2 50-55
Mucosa
Mucosa
Laugier-Hunziker sendromu, mukokutanöz lentijinler ve melanonişiyle seyreden nadir görülen kalıtsal bir pigment bozukluğudur. Bu sendroma, altta yatan bir malignite ya da sistemik hastalıkla henüz ilişkilendirilmediğinden benign olarak yakl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62fc00a5ee87f80319a1ef84d6379651
https://doi.org/10.33204/mucosa.948546
https://doi.org/10.33204/mucosa.948546
Akademický článek
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Publikováno v:
Indian Journal of Dermatology
Indian Journal of Dermatology, Vol 62, Iss 2, Pp 191-194 (2017)
Indian Journal of Dermatology, Vol 62, Iss 2, Pp 191-194 (2017)
Introduction: Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive potentially life-threatening condition, characterized by glucocorticoid deficiency, preserved aldosterone/renin secretion, and secondary rise in plasma adrenocortico
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a388055a3dc1e588feac2f45f940391
http://europepmc.org/articles/PMC5363144
http://europepmc.org/articles/PMC5363144
Autor:
Daniel López-Moreno, Enriqueta Hofmann, Juan Carlos Zenteno, Oscar F. Chacon-Camacho, Vianney Cortés-González, Cristina Villanueva-Mendoza, Ilse Wieland, Michelle Pacheco‐Quito, Martha Alejandra Morales-Sánchez, Martin Zenker
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Postzygotic KRAS, HRAS, NRAS, and FGFR1 mutations result in a group of mosaic RASopathies characterized by related developmental anomalies in eye, skin, heart, and brain. These oculocutaneous disorders include oculoectodermal syndrome (OES
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42c7f6b337abcd9f47de9ea9584e88e
https://doi.org/10.1002/mgg3.625
https://doi.org/10.1002/mgg3.625
Akademický článek
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Akademický článek
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Publikováno v:
Türkderm, Vol 45, Iss 3, Pp 158-160 (2011)
WOS: 000295572800010
Laugier-Hunziker syndrome (LHS) is a rare, acquired mucocutaneous hyperpigmentation often associated with longitudinal melanonychia. It is important to differentiate this condition from the pigmentary disorders of the oral m
Laugier-Hunziker syndrome (LHS) is a rare, acquired mucocutaneous hyperpigmentation often associated with longitudinal melanonychia. It is important to differentiate this condition from the pigmentary disorders of the oral m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e8e224d3e41f2ae818a92bdeb15c241f
http://www.journalagent.com/z4/download_fulltext.asp?pdir=turkderm&plng=eng&un=TURKDERM-05668
http://www.journalagent.com/z4/download_fulltext.asp?pdir=turkderm&plng=eng&un=TURKDERM-05668