Abstract
The case history of a set of twins with Rett syndrome is presented. The twins test as monozygotic by both blood groups and HLA titers. In a previous generation, the family had three females who died of an unknown degenerative disease on the paternal side of this family. The discussion includes a hypothesis about female genetic disease occurring in a recessive pattern on the X chromosome.
Original language | English (US) |
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Pages (from-to) | 475-478 |
Number of pages | 4 |
Journal | Brain and Development |
Volume | 9 |
Issue number | 5 |
DOIs | |
State | Published - Jan 1 1987 |
Keywords
- Rett syndrome
- female X-linked disease
- monozygotic twins
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Developmental Neuroscience
- Clinical Neurology