Literature DB >> 22931192

The Medich giant platelet syndrome: two new cases.

William Gunning1, Mukund Dole, Martin Brecher, James G White.   

Abstract

Hypogranular platelet disorders in human subjects are relatively rare. They include the gray platelet syndrome, αδ storage pool deficiency, the Hermansky-Pudlak syndrome, and the white platelet syndrome. Perhaps the rarest of them all is the Medich giant platelet disorder. No additional cases of this condition have been reported since description of the first case in 2004. This study describes two children with thrombocytopenia and giant, hypogranular platelets found shortly after birth. Electron microscopic study of their platelets revealed sheets of membrane wrapped into tubes resembling scrolls. The scroll-like structures were open at both ends and often filled with glycogen particles. The abnormal structures are identical to those found in the initial case. As a result, the disorder can now be referred to as the Medich giant platelet syndrome.

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Year:  2012        PMID: 22931192     DOI: 10.3109/09537104.2012.671980

Source DB:  PubMed          Journal:  Platelets        ISSN: 0953-7104            Impact factor:   3.862


  2 in total

1.  Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia.

Authors:  Eva Leinøe; Eva Zetterberg; Savvas Kinalis; Olga Østrup; Peter Kampmann; Eva Norström; Nadine Andersson; Jenny Klintman; Klaus Qvortrup; Finn Cilius Nielsen; Maria Rossing
Journal:  Br J Haematol       Date:  2017-07-27       Impact factor: 6.998

2.  Using Cryo-ET to distinguish platelets during pre-acute myeloid leukemia from steady state hematopoiesis.

Authors:  Yuewei Wang; Tong Huo; Yu-Jung Tseng; Lan Dang; Zhili Yu; Wenjuan Yu; Zachary Foulks; Rebecca L Murdaugh; Steven J Ludtke; Daisuke Nakada; Zhao Wang
Journal:  Commun Biol       Date:  2022-01-20
  2 in total

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