Gottron’s acrogeria and peliosis hepatis
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Peertechz Publications Private Limited
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https://www.peertechzpublications.com/articles/GJRD-4-117.pdf
Reference25 articles.
1. 1. Jansen T, de Paepe A, Luytinck N, Plewig G (2000) COL3A1 mutation leading to acrogeria (Gottron Type). Br J Dermatol 142: 178-180. Link: http://bit.ly/2rxizmJ
2. 2. Bruckner-Tuderman L, Vogel A, Schnyder UW (1987) Fibroblasts of an acrogeria patient produce normal amounts of type I and III collagen. Dermatologica 174: 157-165. Link: http://bit.ly/36OqJHn
3. 3. Gilkes JJ, Sharvill DE, Wells RS (1974) The premature ageing syndromes. Report of eight cases and description of a new entity named metageria. Br J Dermatol 91: 243-262. Link: http://bit.ly/33CKu2y
4. 4. Maroofian R, Murdocca M, Rezaei-Delui H, Nekooei A, Mojarad M, et al. (2018) A novel in-frame deletion in ZMPSTE24 is associated with autosomal recessive acrogeria (Gottron type) in an extended consanguineous family. Clin Dysmorphol 27: 88-90. Link: http://bit.ly/2Q5CBir
5. 5. Blaszczyk M, Depaepe A, Nuytinck L, Glinska-Ferenz M, Jablonska S (2000) Acrogeria of the Gottron type in a mother and son. Eur J Dermatol 10: 36-40. Link: http://bit.ly/2pQL0f1
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