The small, spastic, and furrowed tongue of Allgrove syndrome

Neurology

Volumn 72, Issue 15, 2009, Pages 1366-

  Houlden, Henry ^a  

^a NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLGROVE SYNDROME; ARTICLE; CASE REPORT; CLINICAL FEATURE; DNA DETERMINATION; GENE MUTATION; HUMAN; MALE; PRIORITY JOURNAL; TONGUE DISEASE; ADRENAL CORTEX DISEASE; ESOPHAGUS ACHALASIA; GENETICS; LACRIMAL GLAND DISEASE; MUSCLE SPASM; MUTATION; PATHOLOGY; PEDIGREE; PHYSIOLOGY; PROGRESSIVE BULBAR PALSY; SYNDROME; TONGUE;

AAAS PROTEIN, HUMAN; NERVE PROTEIN; NUCLEOPORIN;

ADRENAL CORTEX DISEASES; ADULT; BULBAR PALSY, PROGRESSIVE; ESOPHAGEAL ACHALASIA; HUMANS; LACRIMAL APPARATUS DISEASES; MALE; MUTATION; NERVE TISSUE PROTEINS; NUCLEAR PORE COMPLEX PROTEINS; PEDIGREE; SPASM; SYNDROME; TONGUE; TONGUE DISEASES;

EID: 65349104761     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3181a0fe97     Document Type: Note

References (2)

1. Tullio-Pelet A, Salomon R, Hadj-Rabia S, et al. Mutant WD-repeat protein in triple-A syndrome. Nat Genet 2000;26:332-335.
2. Houlden H, Smith S, De Carvalho M, et al. Clinical and genetic characterization of families with triple A (Allgrove) syndrome. Brain 2002;125:2681-2690.