Angioma‐sepiginosum‐like and hyperkeratotic lesion in a patient with Goltz syndrome

Author(s):  
Angel Fernandez‐Flores ◽  
Sabela Paradela ◽  
Jesús del Pozo ◽  
Nieves Martínez‐Campayo ◽  
David Cassarino ◽  
...  

2011 ◽  
Vol 7 (1) ◽  
Author(s):  
Ana R Casaroto ◽  
Daniela CN Rocha Loures ◽  
Eduardo Moreschi ◽  
Vanessa C Veltrini ◽  
Cleverson L Trento ◽  
...  


2018 ◽  
Vol 30 (5) ◽  
pp. 597
Author(s):  
Shih-Wen Hsu ◽  
Chien-yio Lin ◽  
Chuang-Wei Wang ◽  
Wen-Hung Chung ◽  
Chih-Hsun Yang ◽  
...  
Keyword(s):  


2002 ◽  
Vol 39 (4) ◽  
pp. 469-473 ◽  
Author(s):  
Jeffrey A. Ascherman ◽  
Sean L. Knowles ◽  
Kenneth C. Troutman

Objective Goltz syndrome is a rare, X-linked dominant, multisystem disorder found almost exclusively in female patients. Although the cutaneous features predominate in most reports, characteristic abnormalities are also frequently present in the musculoskeletal system and facial region. We report a female infant born with a severe form of Goltz syndrome that included an extremely wide facial cleft, an abnormality not previously reported in a patient with this disorder. Her management demonstrates the advantages of a multidisciplinary approach to effectively care for patients with severe craniofacial abnormalities.



Dermatology ◽  
2010 ◽  
Vol 220 (1) ◽  
pp. 57-59 ◽  
Author(s):  
Tatiana Lamon ◽  
Stephane Gerard ◽  
Nicolas Meyer ◽  
Benjamin Losfeld ◽  
Gabor Abellan van Kan ◽  
...  




2020 ◽  
Vol 86 (6) ◽  
pp. 691
Author(s):  
Zhimiao Lin ◽  
Zijuan Wang ◽  
Huijun Wang


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Carvalho Sérgio Henrique Gonçalves de ◽  
Pereira Joabe dos Santos ◽  
Agripino Gustavo Gomes ◽  
Góes Pedro Everton Marques ◽  
Marinho Sandra Aparecida
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