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X-linked lymphoproliferative disease: prenatal detection of an unaffected histocompatible male

✍ Scribed by J. C. Mulley; A. M. Turner; A. K. Gedeon; V. A. Berdoukas; T. H. M. Huang; D. H. Ledbetter; H. Grierson; D. T. Purtilo

Book ID
115090296
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
454 KB
Volume
42
Category
Article
ISSN
0009-9163

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## Abstract A family study was performed in order to diagnose X‐linked lymphoproliferative (XLP) disease in a fetus. The molecular genetic analysis indicated that the fetus, as well as its healthy 7‐year‐old brother, inherited XLP. Analysis of immunoglobulin subclasses from the 7‐year‐old brother s