Ontology highlight
ABSTRACT:
SUBMITTER: Seri M
PROVIDER: S-EPMC1377769 | biostudies-other | 1999 Feb
REPOSITORIES: biostudies-other
Seri M M Cusano R R Forabosco P P Cinti R R Caroli F F Picco P P Bini R R Morra V B VB De Michele G G Lerone M M Silengo M M Pela I I Borrone C C Romeo G G Devoto M M
American journal of human genetics 19990201 2
We have recently observed a large pedigree with a new rare autosomal dominant spastic paraparesis. In three subsequent generations, 13 affected individuals presented with bilateral cataracts, gastroesophageal reflux with persistent vomiting, and spastic paraparesis with amyotrophy. Bilateral cataracts occurred in all affected individuals, with the exception of one patient who presented with a chorioretinal dystrophy, whereas clinical signs of spastic paraparesis showed a variable expressivity. U ...[more]