𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Autosomal recessive primary generalized dystonia in two siblings from a consanguineous family

✍ Scribed by Paolo Moretti; Peter Hedera; John Wald; John Fink


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
53 KB
Volume
20
Category
Article
ISSN
0885-3185

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

We describe the clinical features of a brother and sister with non–dopa‐responsive, childhood‐onset, generalized dystonia. The children were born to consanguineous parents, had no family history of neurologic disease, no evidence of structural or metabolic causes of dystonia, and negative testing for the GAG946 deletion mutation in the DYT1 gene. This report supports the existence of a generalized type of dystonia with autosomal recessive inheritance (DYT2). © 2004 Movement Disorder Society