Výsledky vyhledávání - "Syndrome In Question"

Do you know this syndrome? Schimmelpenning-Feuerstein-Mims syndrome

Autor: Lena, Clarissa Patias, Kondo, Rogério Nabor, Nicolacópulos, Théo

Publikováno v: Anais Brasileiros de Dermatologia, Vol 94, Iss 2, Pp 227-229 (2019)
Anais Brasileiros de Dermatologia

Nevus sebaceous is the most common type of organoid epidermal nevus, often located on the face, following the Blaschko's lines and with alterations in the ipsilateral central nervous system. Distinct disorders can be distinguished by the type of asso

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cdcf937a14dac8f26c399f4dc1dfa28
https://doi.org/10.1590/abd1806-4841.20197661

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Do you know this syndrome? Ichthyosis associated with neurological condition and alteration of hairs

Autor: Neusa Yuriko Sakai Valente, Luciana Baptista Pereira, Vanessa Barreto Rocha

Publikováno v: Anais Brasileiros de Dermatologia, Vol 93, Iss 1, Pp 135-137 (2018)
Anais Brasileiros de Dermatologia v.93 n.1 2018
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD
Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia, Volume: 93, Issue: 1, Pages: 135-137, Published: FEB 2018

Trichothiodystrophy refers to a heterogeneous group of rare genetic diseases that affects neuroectodermal-derived tissues with multisystem involvement. The hallmark of these syndromes is the deficiency of sulfur in hair matrix proteins, leading to sh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::697a54215f3d0137651b27daae7b35cc
http://www.scielo.br/pdf/abd/v93n1/0365-0596-abd-93-01-0135.pdf

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Do you know this syndrome? Leopard syndrome*

Autor: Dauro Douglas Oliveira, Luis Candido Pinto da Silva, Ana Carolina Dias Viana de Andrade, Flávio Heleno da Silva Queiroz Cançado, Paulo Franco Taitson, Matheus Melo Pithon

Publikováno v: Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia, Vol 92, Iss 1, Pp 127-129 (2017)

Hypertrophic cardiomyopathy is known as Leopard syndrome, which is a mnemonic rule for multiple lentigines (L), electrocardiographic conduction abnormalities (E), ocular hypertelorism (O), pulmonary stenosis (P), abnormalities of genitalia (A), retar

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59d136d4491c58ca02570342aadcc001
http://europepmc.org/articles/PMC5312195

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Do you know this syndrome? Hand-foot syndrome*

Autor: Juliana Polizel Ocanha, Rafael Bispo Paschoalini, Cintia Santos Braghiroli, Hélio Amante Miot, Rodrigo Ieiri

Publikováno v: Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia, Vol 92, Iss 1, Pp 131-133 (2017)
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP

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Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e328d3b1190feac5839eb30eca1a433e
http://europepmc.org/articles/PMC5312196

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Syndrome in question: antisynthetase syndrome (anti-PL-7)

Autor: Hélio Amante Miot, Tatiana Cristina Gige, Ana Cláudia Cavalcante Espósito

Publikováno v: Anais Brasileiros de Dermatologia, Vol 91, Iss 5, Pp 683-685 (2016)
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Anais Brasileiros de Dermatologia

Made available in DSpace on 2018-12-11T17:30:08Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-09-01. Added 1 bitstream(s) on 2021-07-15T15:04:09Z : No. of bitstreams: 1 S0365-05962016000500683.pdf: 279510 bytes, checksum: 8d7116175f507b3af29

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85d93db7e482840ba611bfc364385849
https://doi.org/10.1590/abd1806-4841.20164449

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Syndrome in question: Gorlin-Goltz syndrome

Autor: Karina Demoner de Abreu, Pauline Lyrio Ribeiro, João Basilio de Souza Filho, Christine Chambo Pignaton, Marisa Simon Brezinscki

Publikováno v: Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia, Vol 91, Iss 4, Pp 541-543 (2016)

The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) is an uncommon disorder caused by a mutation in Patched, tumor suppressor gene. It is mainly characterized by numerous early onset basal cell carcinomas, odontogenic cysts of jaw and skeletal abnormali

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba64c19bf079a85ea9ff66c48615f255
https://doi.org/10.1590/abd1806-4841.20164428

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Do you know this syndrome? Harlequin syndrome

Autor: Hans-Bittner, Nelise Ritter, Bittner, Guilherme Canho, Hans Filho, Günter

Publikováno v: Anais Brasileiros de Dermatologia, Vol 93, Iss 4, Pp 585-586 (2018)
Anais Brasileiros de Dermatologia

Harlequin syndrome is a rare condition in which one half of the face fails to flush and sweat due to damage of the sympathetic fibers on the ipsilateral side. The majority of cases are idiopathic, but may be iatrogenic or caused by space-occupying le

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f9d9fc89a4d58388bb332b48ed8fc70
https://doi.org/10.1590/abd1806-4841.20187549

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Syndrome in question

Autor: Priscila Regina Orso Rebellato, Camila Makino Rezende, Eveline Roesler Battaglin, Brunno Zeni de Lima, Jose Fillus Neto

Publikováno v: Anais Brasileiros de Dermatologia, Vol 90, Iss 6, Pp 909-911 (2015)
Anais Brasileiros de Dermatologia

Morbihan Syndrome is a rare entity with unknown etiology. It is clinically characterized by chronic erythematous edema on the face - especially in the middle and upper third of the face - and creates abnormal facial contours that are initially interm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd314c5e456c22e4aeb70e37c8249f32
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000600909&tlng=en

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SYNDROME IN QUESTION

Autor: Nilton Di Chiacchio, Julio Cesar Jasso-Olivares, Nilton Gioia Di Chiacchio, José Antonio Jacinto, Maria Victoria Suárez Restrepo

Publikováno v: Anais Brasileiros de Dermatologia, Vol 90, Iss 3, Pp 423-425 (2015)
Anais Brasileiros de Dermatologia

The Iso-Kikuchi Syndrome is a rare condition characterized by nail dysplasia involving the index fingers, including micronychia, polyonychia, anonychia, irregular lunula, malalignment and hemionychogryphosis. On the antero-posterior image, radiologic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21edcf6d55075ad9cebfbbed98017ab7
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000300423&tlng=en

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Syndrome In Question*

Autor: Gabriela Maldonado, Juliano Peruzzo, Clarissa Prieto Herman Reinehr, Gabriela Fortes Escobar, Mariana Quirino Tubone

Publikováno v: Anais Brasileiros de Dermatologia
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Anais Brasileiros de Dermatologia, Vol 89, Iss 4, Pp 679-680 (2014)
Anais Brasileiros de Dermatologia, Vol 90, Iss 1, Pp 131-133 (2015)
Anais Brasileiros de Dermatologia, Vol 90, Iss 4, Pp 589-590 (2015)
Anais Brasileiros de Dermatologia, Vol 89, Iss 1, Pp 175-176 (2014)
Anais Brasileiros de Dermatologia, Vol 90, Iss 5, Pp 759-761 (2015)

The authors describe a case of Cowden´s syndrome in a female patient with classic cutaneous lesions, plus papillomatous lesions in the gastrointestinal tract and a previous history of thyroid carcinoma. Mucocutaneous lesions occur in 90% of Cowden's

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f916a33e104dd815d8a377a4b96a067
http://europepmc.org/articles/PMC4323714

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