Gottron's acrogeria and peliosis hepatis

<p>We report the case of a 62-year-old woman with Gottron's acrogeria and peliosis hepatis. Gottron's acrogeria is a rare congenital disease characterized by atrophic acral skin with mottled hyperpigmentation and an aged appearance. It is mostly caused by a mutation in COL3A1 gene th...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Gloria Cobo Ramírez (Yazar), Monica Lopez Rodriguez (Yazar), Andres Gonzalez Garcia (Yazar), Marta Rosas Cancio-Suarez (Yazar), Luis Adrian Viteri (Yazar), Luis Manzano Espinosa (Yazar)
Materyal Türü: Kitap
Baskı/Yayın Bilgisi: Global Journal of Rare Diseases - Peertechz Publications, 2019-11-12.
Konular:
Online Erişim:Connect to this object online.
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

MARC

LEADER 00000 am a22000003u 4500
001 peertech__10_17352_2640-7876_000017
042 |a dc 
100 1 0 |a Gloria Cobo Ramírez  |e author 
700 1 0 |a  Monica Lopez Rodriguez  |e author 
700 1 0 |a  Andres Gonzalez Garcia  |e author 
700 1 0 |a  Marta Rosas Cancio-Suarez  |e author 
700 1 0 |a  Luis Adrian Viteri  |e author 
700 1 0 |a Luis Manzano Espinosa  |e author 
245 0 0 |a Gottron's acrogeria and peliosis hepatis 
260 |b Global Journal of Rare Diseases - Peertechz Publications,   |c 2019-11-12. 
520 |a <p>We report the case of a 62-year-old woman with Gottron's acrogeria and peliosis hepatis. Gottron's acrogeria is a rare congenital disease characterized by atrophic acral skin with mottled hyperpigmentation and an aged appearance. It is mostly caused by a mutation in COL3A1 gene that leads to defective production of type III collagen.</p> 
540 |a Copyright © Gloria Cobo Ramírez et al. 
546 |a en 
655 7 |a Case Report  |2 local 
856 4 1 |u https://doi.org/10.17352/2640-7876.000017  |z Connect to this object online.