Literature DB >> 8412004

Decreased blood coagulation activities in carbohydrate-deficient glycoprotein syndrome.

N Okamoto1, Y Wada, M Kobayashi, K Otani, T Tagawa, Y Futagi, Y Imayoshi, A Hayashi, A Shimizu, Y Kato.   

Abstract

The carbohydrate-deficient glycoprotein (CDG) syndromes are a newly recognized group of inherited metabolic diseases. We report a Japanese brother and sister with a CDG syndrome. Both patients showed decreased activities of blood coagulation Factor XI and of the coagulation inhibitor protein C. In one of them there was also a somewhat decreased activity of Factor IX and of antithrombin III. Isoelectric focusing of antithrombin III revealed a decrease of negatively charged fractions and an increase of more cathodal bands. Furthermore, there was a discrepancy between activity and antigen level of Factor VIII and protein C. The patients had an incidental deficiency of factor XII. This is the first detailed report on blood coagulation systems in the CDG syndromes. These blood coagulation abnormalities may explain at least in part the thrombotic or haemorrhagic complications of the CDG syndromes.

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Year:  1993        PMID: 8412004     DOI: 10.1007/bf00710294

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  7 in total

1.  A new variant of the carbohydrate deficient glycoproteins syndrome.

Authors:  V T Ramaekers; H Stibler; J Kint; J Jaeken
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

2.  The carbohydrate deficient glycoprotein syndrome in three Japanese children.

Authors:  K Ohno; I Yuasa; S Akaboshi; M Itoh; K Yoshida; H Ehara; Y Ochiai; K Takeshita
Journal:  Brain Dev       Date:  1992-01       Impact factor: 1.961

3.  Disialotransferrin developmental deficiency syndrome.

Authors:  B Kristiansson; M Andersson; B Tonnby; B Hagberg
Journal:  Arch Dis Child       Date:  1989-01       Impact factor: 3.791

4.  A new procedure for the determination of transferrin C (Tf C) subtypes by isoelectric focusing. Existence of two additional alleles, Tf C4 and Tf C5.

Authors:  J Constans; P Kühnl; M Viau; W Spielmann
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  Development of the human coagulation system in the full-term infant.

Authors:  M Andrew; B Paes; R Milner; M Johnston; L Mitchell; D M Tollefsen; P Powers
Journal:  Blood       Date:  1987-07       Impact factor: 22.113

6.  Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome.

Authors:  J Jaeken; H G van Eijk; C van der Heul; L Corbeel; R Eeckels; E Eggermont
Journal:  Clin Chim Acta       Date:  1984-12-29       Impact factor: 3.786

7.  Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome.

Authors:  H Stibler; J Jaeken
Journal:  Arch Dis Child       Date:  1990-01       Impact factor: 3.791

  7 in total
  3 in total

1.  Analysis of serum protein precipitated with antiserum by matrix-assisted laser desorption ionization/time-of-flight and electrospray ionization mass spectrometry as a clinical laboratory test.

Authors:  T Nakanishi; A Shimizu; N Okamoto; A Ingendoh; M Kanai
Journal:  J Am Soc Mass Spectrom       Date:  1995-09       Impact factor: 3.109

2.  High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency).

Authors:  S Grünewald; E Schollen; E Van Schaftingen; J Jaeken; G Matthijs
Journal:  Am J Hum Genet       Date:  2001-01-11       Impact factor: 11.025

3.  Proteome-wide analysis of single-nucleotide variations in the N-glycosylation sequon of human genes.

Authors:  Raja Mazumder; Krishna Sudeep Morampudi; Mona Motwani; Sona Vasudevan; Radoslav Goldman
Journal:  PLoS One       Date:  2012-05-07       Impact factor: 3.240

  3 in total

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