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Favier, R., Jondeau, K., Boutard, P., Grossfeld, P., Reinert, P., Jones, C., et al. (2003) Paris-Trousseau Syndrome: Clinical, Hematological, Molecular Data of Ten New Cases. Thrombosis and Haemostasis, 90, 893-897.
http://dx.doi.org/10.1160/TH03-02-0120

has been cited by the following article:

• TITLE: Jacobsen/Paris-Trousseau Syndrome: Report of a Case with Emphasis on Platelet’s Light Microscopic and Ultrastructure Findings

  AUTHORS: Michael Losos, Basil M. Kahwash, Miriam Conces, Joel Thompson, Riten Kumar, Samir B. Kahwash

  KEYWORDS: Jacobsen Syndrome, Paris-Trousseau Syndrome, Platelet Microscopic Findings, Electron Microscopy

  JOURNAL NAME: Open Journal of Pathology, Vol.6 No.1, January 6, 2016

  ABSTRACT: Jacobsen syndrome (JS) is a rare, inherited disorder, characterized by facial and skull dysmorphism, mental retardation, and platelet abnormalities. Paris-Trousseau syndrome (PTS) is a platelet function disorder that may be encountered in patients affected by JS. PTS is manifested by a mild lifelong bleeding tendency. Morphologically, the presence of large fused platelet alpha granules is characteristic. We present a case of Jacobsen syndrome in a child and highlight the typical morphologic and ultrastructure findings of platelets.