Literature DB >> 8495043

Hereditary lipo-muscular atrophy with joint contracture, skin eruptions and hyper-gamma-globulinemia: a new syndrome.

M Tanaka1, N Miyatani, S Yamada, K Miyashita, I Toyoshima, K Sakuma, K Tanaka, T Yuasa, T Miyatake, T Tsubaki.   

Abstract

We previously reported two siblings with decreased subcutaneous adipose tissue, muscular atrophy, joint contractures, recurrent skin eruptions, hyper-gamma-globulinemia, and reduced natural killer cell activity. Some of their clinical features are similar to those of partial lipodystrophy, but they are distinct in that muscular atrophy, joint contractures and recurrent skin eruptions are not found in patients with partial lipodystrophy. Thirteen other Japanese patients with similar clinical manifestations have been reported. We propose that such cases should be considered a distinct clinical entity.

Entities:  

Mesh:

Year:  1993        PMID: 8495043     DOI: 10.2169/internalmedicine.32.42

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  12 in total

1.  An autosomal recessive syndrome of joint contractures, muscular atrophy, microcytic anemia, and panniculitis-associated lipodystrophy.

Authors:  Abhimanyu Garg; Maria Dolores Hernandez; Ana Berta Sousa; Lalitha Subramanyam; Laura Martínez de Villarreal; Heloísa G dos Santos; Oralia Barboza
Journal:  J Clin Endocrinol Metab       Date:  2010-06-09       Impact factor: 5.958

2.  Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity.

Authors:  Yin Liu; Yuval Ramot; Antonio Torrelo; Amy S Paller; Nuo Si; Sofia Babay; Peter W Kim; Afzal Sheikh; Chyi-Chia Richard Lee; Yongqing Chen; Angel Vera; Xue Zhang; Raphaela Goldbach-Mansky; Abraham Zlotogorski
Journal:  Arthritis Rheum       Date:  2012-03

3.  CANDLE Syndrome: orodfacial manifestations and dental implications.

Authors:  T Roberts; L Stephen; C Scott; T di Pasquale; A Naser-Eldin; M Chetty; S Shaik; L Lewandowski; P Beighton
Journal:  Head Face Med       Date:  2015-12-28       Impact factor: 2.151

Review 4.  Immunology in clinic review series; focus on autoinflammatory diseases: update on monogenic autoinflammatory diseases: the role of interleukin (IL)-1 and an emerging role for cytokines beyond IL-1.

Authors:  R Goldbach-Mansky
Journal:  Clin Exp Immunol       Date:  2012-03       Impact factor: 4.330

5.  A mutation in the immunoproteasome subunit PSMB8 causes autoinflammation and lipodystrophy in humans.

Authors:  Akiko Kitamura; Yoichi Maekawa; Hisanori Uehara; Keisuke Izumi; Izumi Kawachi; Masatoyo Nishizawa; Yasuko Toyoshima; Hitoshi Takahashi; Daron M Standley; Keiji Tanaka; Jun Hamazaki; Shigeo Murata; Koji Obara; Itaru Toyoshima; Koji Yasutomo
Journal:  J Clin Invest       Date:  2011-09-01       Impact factor: 14.808

6.  PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome.

Authors:  Anil K Agarwal; Chao Xing; George N DeMartino; Dario Mizrachi; Maria Dolores Hernandez; Ana Berta Sousa; Laura Martínez de Villarreal; Heloísa G dos Santos; Abhimanyu Garg
Journal:  Am J Hum Genet       Date:  2010-12-10       Impact factor: 11.025

7.  Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome.

Authors:  Kazuhiko Arima; Akira Kinoshita; Hiroyuki Mishima; Nobuo Kanazawa; Takeumi Kaneko; Tsunehiro Mizushima; Kunihiro Ichinose; Hideki Nakamura; Akira Tsujino; Atsushi Kawakami; Masahiro Matsunaka; Shimpei Kasagi; Seiji Kawano; Shunichi Kumagai; Koichiro Ohmura; Tsuneyo Mimori; Makito Hirano; Satoshi Ueno; Keiko Tanaka; Masami Tanaka; Itaru Toyoshima; Hirotoshi Sugino; Akio Yamakawa; Keiji Tanaka; Norio Niikawa; Fukumi Furukawa; Shigeo Murata; Katsumi Eguchi; Hiroaki Ida; Koh-Ichiro Yoshiura
Journal:  Proc Natl Acad Sci U S A       Date:  2011-08-18       Impact factor: 11.205

Review 8.  Insights from Mendelian Interferonopathies: Comparison of CANDLE, SAVI with AGS, Monogenic Lupus.

Authors:  Hanna Kim; Gina A Montealegre Sanchez; Raphaela Goldbach-Mansky
Journal:  J Mol Med (Berl)       Date:  2016-09-27       Impact factor: 4.599

Review 9.  Untangling the web of systemic autoinflammatory diseases.

Authors:  Donato Rigante; Giuseppe Lopalco; Antonio Vitale; Orso Maria Lucherini; Francesco Caso; Caterina De Clemente; Francesco Molinaro; Mario Messina; Luisa Costa; Mariangela Atteno; Franco Laghi-Pasini; Giovanni Lapadula; Mauro Galeazzi; Florenzo Iannone; Luca Cantarini
Journal:  Mediators Inflamm       Date:  2014-07-15       Impact factor: 4.711

10.  Genetics of proteasome diseases.

Authors:  Aldrin V Gomes
Journal:  Scientifica (Cairo)       Date:  2013-12-30
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.