Abstract
Cerebrotendinous xanthomatosis (CTX), is one of the few autosomal recessive progressive storage diseases allowing affected individuals to reproduce. We investigated 38 CTX patients and most of their families. The possibility of a high risk situation for the fetus and/or the apparently healthy newborn infant born to CTX mothers and female carriers of the gene is discussed for genetic counseling purposes and in view of available treatment.
Original language | English |
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Pages (from-to) | 11-16 |
Number of pages | 6 |
Journal | American Journal of Medical Genetics |
Volume | 31 |
Issue number | 1 |
DOIs | |
State | Published - 1 Jan 1988 |
ASJC Scopus subject areas
- Genetics(clinical)