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...
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| Main Authors: | , , , , , |
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| Format: | Book |
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Global Journal of Rare Diseases - Peertechz Publications,
2019-11-12.
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| 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. |