Literature DB >> 4026345

A syndrome with nodular erythema, elongated and thickened fingers, and emaciation.

Y Kitano, E Matsunaga, T Morimoto, N Okada, S Sano.   

Abstract

A 5-year-old boy had a nodular erythema, elongated and thickened fingers, and emaciation. His condition was a rare congenital disease inherited as an autosomal recessive trait. Eleven cases have been previously reported in the Japanese literature. The onset is early in childhood, and nodular erythema is an essential and initial finding. Growth retardation and emaciation progress slowly with age. The characteristic clinical features include large eyes, nose, lips, and ears, disproportionately long and thick fingers, and the loss of adipose tissue from the upper half of the body. Cardiomegaly and hypertrophy of the periosteum of the phalanges have been described in some cases.

Entities:  

Mesh:

Year:  1985        PMID: 4026345

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  10 in total

1.  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

2.  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 3.  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

4.  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

5.  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 6.  Proteostasis Perturbations and Their Roles in Causing Sterile Inflammation and Autoinflammatory Diseases.

Authors:  Jonas Johannes Papendorf; Elke Krüger; Frédéric Ebstein
Journal:  Cells       Date:  2022-04-22       Impact factor: 7.666

Review 7.  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

8.  Nakajo-Nishimura syndrome and related proteasome-associated autoinflammatory syndromes.

Authors:  Koichiro Ohmura
Journal:  J Inflamm Res       Date:  2019-09-17

9.  Genetics of proteasome diseases.

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

Review 10.  Type I interferonopathies in pediatric rheumatology.

Authors:  Stefano Volpi; Paolo Picco; Roberta Caorsi; Fabio Candotti; Marco Gattorno
Journal:  Pediatr Rheumatol Online J       Date:  2016-06-04       Impact factor: 3.054

  10 in total

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