Triple A syndrome

Indian Journal of Gastroenterology

Volumn 24, Issue 5, 2005, Pages 217-218

  Bharadia, Lalit ^a   Kalla, Mukesh ^a   Sharma, S K ^a   Charan, Rohit ^a   Gupta, J B ^a   Khan, Firoz ^a  

^a S R Kalla Memorial Gastro and General Hospital   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ARTIFICIAL TEAR; HYDROCORTISONE; NITRIC ACID DERIVATIVE; STEROID; AAAS PROTEIN, HUMAN; NUCLEOPORIN; PROTEIN;

ALLGROVE SYNDROME; ARTICLE; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; DYSPHAGIA; ECHOGRAPHY; ESOPHAGUS ACHALASIA; FEMALE; GASTROINTESTINAL ENDOSCOPE; HUMAN; LABORATORY TEST; SCHIRMER TEST; SCHOOL CHILD; ADDISON DISEASE; CHILD; GENETICS; LACRIMAL GLAND DISEASE; MUTATION; SYNDROME;

ADDISON DISEASE; CHILD; ESOPHAGEAL ACHALASIA; FEMALE; HUMANS; LACRIMAL APPARATUS DISEASES; MUTATION; NUCLEAR PORE COMPLEX PROTEINS; PROTEINS; SYNDROME;

EID: 33644789381     PISSN: 02548860     EISSN: 02548860     Source Type: Journal    
DOI: None     Document Type: Article

References (3)

1. Brooks BP, Kleta R, Caruso RC, Stuart C, Ludlow J, Stratakis CA. Triple A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case report. BMC Ophthalmol 2004;4:7.
2. Tuck JS, Bisset RA, Doig CM. Achalasia of the cardia in childhood and the syndrome of achalasia, alacrima and ACTH insensitivity. Clin Radiol 1992;45:427.
3. Ehrich E, Aranoff G, Johnson WG. Familial achalasia associated with adrenocortical insufficiency, alacrima and neurological abnormalities. Am J Med Genet 1987;6:637-44.