Laboratory methods aimed to assess the presence of spheroidal cells such as osmotic fragility, autohemolysis, and glycerol lysis time are very elaborate, time consuming, and often give inconclusive results. We have developed a diagnostic test based on a unique sensitivity of HS cells to hypertonic c
โฆ LIBER โฆ
Modified osmotic fragility test for the laboratory diagnosis of hereditary spherocytosis
โ Scribed by Dr. Luba Judkiewicz; Grzegorz Bartosz; Anna Oplatowska; Andrzej Szczepanek
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 147 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0361-8609
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## Charcot -Marie-Tooth (CMT) disease type 1A is an inherited peripheral neuropathy characterized by slowly progressive distal muscle wasting and weakness, decreased nerve conduction velocities, and genetic linkage to 17p12. Most (>98%) CMT1A cases are caused by a DNA duplication of a 1.5-Mb regio