KEGG   DISEASE: Progressive encephalopathy with amyotrophy and optic atrophy
Entry
H02820                      Disease                                
Name
Progressive encephalopathy with amyotrophy and optic atrophy
Description
Progressive encephalopathy with amyotrophy and optic atrophy (PEAMO) is an early-onset and progressive neurodegenerative encephalopathy with distal spinal muscular atrophy. Mutations in TBCE gene, encoding one of the five tubulin-specific chaperones involved in tubulin folding and polymerization, have been reported from unrelated families.
Category
Nervous system disease
Brite
Human diseases in ICD-11 classification [BR:br08403]
 08 Diseases of the nervous system
  Movement disorders
   8A0Y  Other specified movement disorders
    H02820  Progressive encephalopathy with amyotrophy and optic atrophy
Gene
TBCE [HSA:6905] [KO:K21768]
Other DBs
ICD-11: 8A0Y
OMIM: 617207
Reference
  Authors
Sferra A, Baillat G, Rizza T, Barresi S, Flex E, Tasca G, D'Amico A, Bellacchio E, Ciolfi A, Caputo V, Cecchetti S, Torella A, Zanni G, Diodato D, Piermarini E, Niceta M, Coppola A, Tedeschi E, Martinelli D, Dionisi-Vici C, Nigro V, Dallapiccola B, Compagnucci C, Tartaglia M, Haase G, Bertini E
  Title
TBCE Mutations Cause Early-Onset Progressive Encephalopathy with Distal Spinal Muscular Atrophy.
  Journal
Am J Hum Genet 99:974-983 (2016)
DOI:10.1016/j.ajhg.2016.08.006
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